AnALS2gene mutation causes hereditary spastic paraplegia in a Pakistani kindred-Reference-Cited by-同舟云学术

AnALS2gene mutation causes hereditary spastic paraplegia in a Pakistani kindred

Published:2002-12-31 Issue:1 Volume:53 Page:144-145
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Gros-Louis François,Meijer Inge A.,Hand Collette K.,Dubé Marie-Pierre,MacGregor Daune L.,Seni Marie-Hélène,Devon Rebecca S.,Hayden Michael R.,Andermann Frederick,Andermann Eva,Rouleau Guy A.

Funder

Canadian Institutes of Health Research

MUHC Research Institute studentship

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference5 articles.

1. A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2

2. The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis

3. Infantile-Onset Ascending Hereditary Spastic Paralysis Is Associated with Mutations in the Alsin Gene

4. A New Locus for Autosomal Dominant Pure Spastic Paraplegia, on Chromosome 2q24-q34

5. Vps9, Rabex-5 and DSS4: proteins with weak but distinct nucleotide-exchange activities for Rab proteins11Edited by J. Karn

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