The epidemiology of CuZn-SOD mutations in Germany: a study of 217 families (Q44805375)

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scientific article published on 23 March 2010

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English	The epidemiology of CuZn-SOD mutations in Germany: a study of 217 families	scientific article published on 23 March 2010

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instance of

scholarly article

1 reference

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Europe PubMed Central

PubMed publication ID

20309572

retrieved

6 December 2017

title

The epidemiology of CuZn-SOD mutations in Germany: a study of 217 families (English)

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Europe PubMed Central

PubMed publication ID

20309572

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6 December 2017

main subject

Germany

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author

Albert C. Ludolph

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7

object named as

Albert C Ludolph

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Europe PubMed Central

PubMed publication ID

20309572

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6 December 2017

author name string

Malessa Rabe

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1

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Europe PubMed Central

PubMed publication ID

20309572

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6 December 2017

Ansgar Felbecker

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2

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Europe PubMed Central

PubMed publication ID

20309572

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6 December 2017

Stefan Waibel

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3

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Europe PubMed Central

PubMed publication ID

20309572

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6 December 2017

Peter Steinbach

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Europe PubMed Central

PubMed publication ID

20309572

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6 December 2017

Pia Winter

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5

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Europe PubMed Central

PubMed publication ID

20309572

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6 December 2017

Ulrich Müller

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Europe PubMed Central

PubMed publication ID

20309572

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6 December 2017

publication date

23 March 2010

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Europe PubMed Central

PubMed publication ID

20309572

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6 December 2017

published in

Journal of Neurology

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Europe PubMed Central

PubMed publication ID

20309572

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6 December 2017

volume

257

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Europe PubMed Central

PubMed publication ID

20309572

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6 December 2017

issue

8

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Europe PubMed Central

PubMed publication ID

20309572

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6 December 2017

page(s)

1298-1302

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Europe PubMed Central

PubMed publication ID

20309572

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6 December 2017

cites work

Molecular genetic basis of familial ALS.

1 reference

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Crossref

reference URL

https://api.crossref.org/works/10.1007%2FS00415-010-5512-9

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21 January 2018

D90A heterozygosity in the SOD1 gene is associated with familial and apparently sporadic amyotrophic lateral sclerosis

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Crossref

reference URL

https://api.crossref.org/works/10.1007%2FS00415-010-5512-9

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21 January 2018

Amyotrophic lateral sclerosis and structural defects in Cu,Zn superoxide dismutase

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20309572

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial ALS in Germany: origin of the R115G SOD1 mutation by a founder effect

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20309572

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

CuZn-Superoxide Dismutase in D90A Heterozygotes from Recessive and Dominant ALS Pedigrees

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20309572

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Amyotrophic lateral sclerosis associated with mutations in the CuZn superoxide dismutase gene

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20309572

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autosomal dominant amyotrophic lateral sclerosis: a novel mutation in the Cu/Zn superoxide dismutase-1 gene

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20309572

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical characteristics of familial amyotrophic lateral sclerosis with Cu/Zn superoxide dismutase gene mutations

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20309572

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Superoxide dismutase 1: identification of a novel mutation in a case of familial amyotrophic lateral sclerosis

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20309572

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of new mutations in the Cu/Zn superoxide dismutase gene of patients with familial amyotrophic lateral sclerosis.

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20309572

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in all five exons ofSOD-1 may cause ALS

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20309572

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Erratum: Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20309572

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The genetics of motor neuron diseases

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20309572

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Amyotrophic lateral sclerosis associated with homozygosity for an Asp90Ala mutation in CuZn-superoxide dismutase

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20309572

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clustering of ALS patients in central Italy due to the occurrence of the L84F SOD1 gene mutation

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20309572

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recessively inherited amyotrophic lateral sclerosis: a Germany family with the D90A CuZn-SOD mutation

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20309572

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Copper-zinc superoxide dismutase and amyotrophic lateral sclerosis

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20309572

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Linkage of a gene causing familial amyotrophic lateral sclerosis to chromosome 21 and evidence of genetic-locus heterogeneity

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20309572

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Compound heterozygous D90A and D96N SOD1 mutations in a recessive amyotrophic lateral sclerosis family

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20309572

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mild ALS in Japan associated with novel SOD mutation

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20309572

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sixteen novel mutations in the Cu/Zn superoxide dismutase gene in amyotrophic lateral sclerosis: a decade of discoveries, defects and disputes

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/20309572

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/S00415-010-5512-9

1 reference

stated in

Europe PubMed Central

PubMed publication ID

20309572

retrieved

6 December 2017

PubMed publication ID

20309572

1 reference

stated in

Europe PubMed Central

PubMed publication ID

20309572

retrieved

6 December 2017

 

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