Mapping of a complicated familial spastic paraplegia to locus SPG4 on chromosome 2p. (Q33680138)

28 July 2017

title

Mapping of a complicated familial spastic paraplegia to locus SPG4 on chromosome 2p. (English)

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28 July 2017

Weissenbach J

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28 July 2017

Heinzlef O

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28 July 2017

Paternotte C

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28 July 2017

Mahieux F

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28 July 2017

Prud'homme JF

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28 July 2017

Dien J

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28 July 2017

Madigand M

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28 July 2017

Pouget J

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28 July 2017

Roullet E

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28 July 2017

Hazan J

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28 July 2017

language of work or name

English

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publication date

1 February 1998

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Journal of Medical Genetics

28 July 2017

published in

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28 July 2017

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28 July 2017

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28 July 2017

page(s)

89-93

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Pure hereditary spastic paraplegia.

28 July 2017

cites work

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051209

Phenotype of autosomal dominant spastic paraplegia linked to chromosome 2.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051209

A comprehensive genetic map of the human genome based on 5,264 microsatellites

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051209

Incorrect specification of marker allele frequencies: effects on linkage analysis

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051209

X linked spastic paraplegia (SPG2): clinical heterogeneity at a single gene locus

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051209

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051209

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051209

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051209

Classification of the hereditary ataxias and paraplegias

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051209

Familial spastic paraplegia with epilepsy.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051209

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051209

Etiological heterogeneity in X-linked spastic paraplegia

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051209

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051209

Multisystem involvement of the central nervous system in Strümpell's disease. A neurophysiological and neuropsychological study

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051209

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051209

FAMILIAL AMYOTROPHIC DYSTONIC PARAPLEGIA

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051209

Hereditary spastic paraplegia associated with epilepsy, mental retardation and hearing impairment

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051209

Linkage of 'pure' autosomal recessive familial spastic paraplegia to chromosome 8 markers and evidence of genetic locus heterogeneity.

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051209

Familial spastic paraplegia with mental impairment and thin corpus callosum

30 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1051209

The phenotype of "pure" autosomal dominant spastic paraplegia

10 December 2018

1 reference

12 December 2020

Linkage of a new locus for autosomal dominant familial spastic paraplegia to chromosome 2p

1 reference

12 December 2020

Linkage of a locus for autosomal dominant familial spastic paraplegia to chromosome 2p markers

1 reference

12 December 2020

Autosomal dominant spastic paraplegia with anticipation maps to a 4-cM interval on chromosome 2p21-p24 in a large German family

1 reference

12 December 2020

Hereditary Spastic Paraplegia with Dementia

1 reference

12 December 2020

Pure familial spastic paraplegia: clinical and genetic analysis of nine Belgian pedigrees

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.35.2.89

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28 July 2017

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28 July 2017

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