(Q24540152)

English

A new locus for autosomal dominant "pure" hereditary spastic paraplegia mapping to chromosome 12q13, and evidence for further genetic heterogeneity

scientific article

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

6 July 2017

A new locus for autosomal dominant "pure" hereditary spastic paraplegia mapping to chromosome 12q13, and evidence for further genetic heterogeneity (English)

1 reference

Europe PubMed Central

6 July 2017

hereditary spastic paraplegia

1 reference

based on heuristic

inferred from title

object named as

E Reid

1

0 references

author name string

A M Dearlove

2

1 reference

Europe PubMed Central

6 July 2017

M Rhodes

3

1 reference

Europe PubMed Central

6 July 2017

D C Rubinsztein

4

1 reference

Europe PubMed Central

6 July 2017

language of work or name

0 references

publication date

1 September 1999

1 reference

Europe PubMed Central

6 July 2017

American Journal of Human Genetics

1 reference

Europe PubMed Central

6 July 2017

65

1 reference

Europe PubMed Central

6 July 2017

757-763

1 reference

Europe PubMed Central

6 July 2017

3

1 reference

Europe PubMed Central

6 July 2017

Novel locus for autosomal dominant hereditary spastic paraplegia, on chromosome 8q

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377983

24 March 2017

Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nuclear-encoded mitochondrial metalloprotease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377983

24 March 2017

A new locus for autosomal recessive hereditary spastic paraplegia maps to chromosome 16q24.3

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377983

24 March 2017

X-linked spastic paraplegia (SPG1), MASA syndrome and X-linked hydrocephalus result from mutations in the L1 gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377983

24 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377983

24 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377983

24 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377983

24 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377983

24 March 2017

The 1993-94 Généthon human genetic linkage map

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377983

24 March 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377983

7 April 2017

Genetic mapping to 10q23.3-q24.2, in a large Italian pedigree, of a new syndrome showing bilateral cataracts, gastroesophageal reflux, and spastic paraparesis with amyotrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377983

27 September 2017

Quality assessment of whole genome mapping data in the refined familial spastic paraplegia interval on chromosome 14q.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377983

27 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377983

27 September 2017

Autosomal dominant pure spastic paraplegia: a clinical, paraclinical, and genetic study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377983

27 September 2017

Pure hereditary spastic paraplegia.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377983

27 September 2017

Molecular genetics of familial spastic paraplegia: a multitude of responsible genes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377983

27 September 2017

Refined genetic mapping and proteolipid protein mutation analysis in X-linked pure hereditary spastic paraplegia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377983

27 September 2017

Hereditary spastic paraplegia: advances in genetic research. Hereditary Spastic Paraplegia Working group

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377983

27 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377983

27 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377983

27 September 2017

A second-generation linkage map of the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377983

27 September 2017

Phenotype of autosomal dominant spastic paraplegia linked to chromosome 2.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377983

30 May 2018

A quantitative study of sensory function in hereditary spastic paraplegia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377983

30 May 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377983

30 May 2018

X-linked spastic paraplegia and Pelizaeus-Merzbacher disease are allelic disorders at the proteolipid protein locus

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377983

28 July 2018

Cognitive impairment in families with pure autosomal dominant hereditary spastic paraparesis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377983

29 November 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1377983

29 November 2018

Modulation of non-templated nucleotide addition by Taq DNA polymerase: primer modifications that facilitate genotyping

1 reference

https://pubmed.ncbi.nlm.nih.gov/10441583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/10441583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Another pedigree with pure autosomal dominant spastic paraplegia (AD-FSP) from Tibet mapping to 14q11.2-q24.3.

1 reference

https://pubmed.ncbi.nlm.nih.gov/10441583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Locus heterogeneity, anticipation and reduction of the chromosome 2p minimal candidate region in autosomal dominant familial spastic paraplegia

1 reference

https://pubmed.ncbi.nlm.nih.gov/10441583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The phenotype of "pure" autosomal dominant spastic paraplegia

1 reference

https://pubmed.ncbi.nlm.nih.gov/10441583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/10441583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/10441583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/10441583

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

1 reference

Europe PubMed Central

6 July 2017

release_o4jrs2r4yzex7gujfxo6g6itd4

0 references

1 reference

Europe PubMed Central

6 July 2017

1 reference

Europe PubMed Central

6 July 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q24540152&oldid=1525953227"