An ALS2 gene mutation causes hereditary spastic paraplegia in a Pakistani kindred
- 31 December 2002
- journal article
- letter
- Published by Wiley in Annals of Neurology
- Vol. 53 (1) , 144-145
- https://doi.org/10.1002/ana.10422
Abstract
No abstract availableFunding Information
- Canadian Institutes of Health Research
- MUHC Research Institute studentship
This publication has 5 references indexed in Scilit:
- Infantile-Onset Ascending Hereditary Spastic Paralysis Is Associated with Mutations in the Alsin GeneAmerican Journal of Human Genetics, 2002
- The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosisNature Genetics, 2001
- A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2Nature Genetics, 2001
- Vps9, Rabex-5 and DSS4: proteins with weak but distinct nucleotide-exchange activities for Rab proteinsJournal of Molecular Biology, 2001
- A New Locus for Autosomal Dominant Pure Spastic Paraplegia, on Chromosome 2q24-q34American Journal of Human Genetics, 2000