Autosomal dominant familial spastic paraplegia: tight linkage to chromosome 15q (Q24672217)

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Language	Label	Description	Also known as
English	Autosomal dominant familial spastic paraplegia: tight linkage to chromosome 15q	scientific article

Statements

instance of

scholarly article

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title

Autosomal dominant familial spastic paraplegia: tight linkage to chromosome 15q (English)

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author name string

J K Fink

series ordinal

1

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C T Wu

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2

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S M Jones

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3

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G B Sharp

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4

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B M Lange

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5

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A Lesicki

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6

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T Reinglass

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7

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T Varvil

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8

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B Otterud

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9

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M Leppert

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10

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language of work or name

English

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publication date

January 1995

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published in

American Journal of Human Genetics

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volume

56

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issue

1

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page(s)

188-92

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cites work

Strümpell's familial spastic paraplegia: genetics and neuropathology

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stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801321

retrieved

7 April 2017

The gene for Machado-Joseph disease maps to human chromosome 14q

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801321

retrieved

7 April 2017

Autosomal dominant familial spastic paraplegia is genetically heterogeneous and one locus maps to chromosome 14q

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801321

retrieved

7 April 2017

Polymorphic DNA region adjacent to the 5' end of the human insulin gene

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801321

retrieved

7 April 2017

Multilocus linkage analysis in humans: detection of linkage and estimation of recombination

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801321

retrieved

7 April 2017

Hereditary (familial) spastic paraplegia; further clinical and pathologic observations.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801321

retrieved

28 September 2017

Genetic recombination events which position the Friedreich ataxia locus proximal to the D9S15/D9S5 linkage group on chromosome 9q.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801321

retrieved

28 September 2017

Hereditary "pure" spastic paraplegia: a study of nine families

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801321

retrieved

28 September 2017

Hereditary "pure" spastic paraplegia: a clinical and genetic study of 22 families

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801321

retrieved

28 September 2017

Etiological heterogeneity in X-linked spastic paraplegia

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801321

retrieved

28 September 2017

A Dutch family with autosomal dominant pure spastic paraparesis (Strümpell's disease).

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801321

retrieved

28 September 2017

Localization of the autosomal dominant HLA-linked spinocerebellar ataxia (SCA1) locus, in two kindreds, within an 8-cM subregion of chromosome 6p

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801321

retrieved

28 September 2017

A second-generation linkage map of the human genome

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801321

retrieved

28 September 2017

Strumpell's pure familial spastic paraplegia: case study and review of the literature

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801321

retrieved

28 September 2017

Hereditary spastic paraplegia in Western Norway.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801321

retrieved

30 May 2018

Linkage studies of X-linked recessive spastic paraplegia using DNA probes.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801321

retrieved

30 May 2018

HEREDITARY SPASTIC PARAPLEGIA.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801321

retrieved

28 November 2018

Charcot-Marie-Tooth Disease Type 1A -- Association with a Spontaneous Point Mutation in the PMP22 Gene

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801321

retrieved

28 November 2018

Hereditary spastic paraplegia with neurogenic bladder disturbances and syndactylia

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801321

retrieved

28 November 2018

The autosomal dominant form of "pure" familial spastic paraplegia: clinical findings and linkage analysis of a large pedigree

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7825577

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

DNA duplication associated with Charcot-Marie-Tooth disease type 1A

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7825577

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The phenotype of "pure" autosomal dominant spastic paraplegia

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7825577

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sphincter involvement in hereditary spastic paraplegia

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7825577

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1002/AJMG.1320560215

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PMC publication ID

1801321

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PubMed publication ID

7825577

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7625443

reason for deprecated rank

incorrect identifier value

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