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:
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- 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
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- A New Locus for Autosomal Dominant Pure Spastic Paraplegia, on Chromosome 2q24-q34American Journal of Human Genetics, 2000