Alexander disease: GFAP mutations unify young and old. (Q48259696)

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English	Alexander disease: GFAP mutations unify young and old.	scientific article

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12849260

retrieved

10 February 2018

reference URL

http://europepmc.org/abstract/MED/12849260

title

Alexander disease: GFAP mutations unify young and old. (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12849260

retrieved

10 February 2018

reference URL

http://europepmc.org/abstract/MED/12849260

main subject

Alexander disease

1 reference

based on heuristic

inferred from title

author name string

Albee Messing

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12849260

retrieved

10 February 2018

reference URL

http://europepmc.org/abstract/MED/12849260

Michael Brenner

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12849260

retrieved

10 February 2018

reference URL

http://europepmc.org/abstract/MED/12849260

publication date

1 February 2003

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12849260

retrieved

10 February 2018

reference URL

http://europepmc.org/abstract/MED/12849260

published in

Lancet Neurology

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12849260

retrieved

10 February 2018

reference URL

http://europepmc.org/abstract/MED/12849260

volume

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12849260

retrieved

10 February 2018

reference URL

http://europepmc.org/abstract/MED/12849260

issue

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12849260

retrieved

10 February 2018

reference URL

http://europepmc.org/abstract/MED/12849260

page(s)

75

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12849260

retrieved

10 February 2018

reference URL

http://europepmc.org/abstract/MED/12849260

cites work

Mutations in GFAP, encoding glial fibrillary acidic protein, are associated with Alexander disease

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS1474-4422%2803%2900301-6

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

GFAP mutations in Alexander disease

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS1474-4422%2803%2900301-6

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Autosomal dominant palatal myoclonus and spinal cord atrophy

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS1474-4422%2803%2900301-6

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Identification of GFAP gene mutation in hereditary adult-onset Alexander's disease

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1016%2FS1474-4422%2803%2900301-6

retrieved

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

DOI

10.1016/S1474-4422(03)00301-6

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12849260

retrieved

10 February 2018

reference URL

http://europepmc.org/abstract/MED/12849260

PubMed publication ID

12849260

1 reference

stated in

Europe PubMed Central

PubMed publication ID

12849260

retrieved

10 February 2018

reference URL

http://europepmc.org/abstract/MED/12849260

 

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