(Q24672397)

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Autosomal dominant familial spastic paraplegia: reduction of the FSP1 candidate region on chromosome 14q to 7 cM and locus heterogeneity

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Autosomal dominant familial spastic paraplegia: reduction of the FSP1 candidate region on chromosome 14q to 7 cM and locus heterogeneity (English)

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author

Jean Weissenbach

series ordinal

9

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author name string

S Gispert

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1

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N Santos

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2

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R Damen

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3

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T Voit

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4

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J Schulz

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5

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T Klockgether

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6

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G Orozco

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7

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F Kreuz

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8

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G Auburger

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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)

183-7

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cites work

Strategies for multilocus linkage analysis in humans

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801298

retrieved

7 April 2017

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

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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=1801298

retrieved

7 April 2017

Hereditary spastic paraparesis. Clinical and genetic data from a large Dutch family

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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=1801298

retrieved

28 September 2017

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

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PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1801298

retrieved

28 September 2017

Hereditary ataxias and paraplegias in Cantabria, Spain. An epidemiological and clinical study.

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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=1801298

retrieved

30 May 2018

Linkage mapping of dopa–responsive dystonia (DRD) to chromosome 14q

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7825576

retrieved

12 December 2020

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Triplet repeats strike again

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stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/7825576

retrieved

12 December 2020

based on heuristic

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PMC publication ID

1801298

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PubMed publication ID

7825576

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(Q24672397)

Autosomal dominant familial spastic paraplegia: reduction of the FSP1 candidate region on chromosome 14q to 7 cM and locus heterogeneity

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