| Literature DB >> 11835381 |
Philippe Corcia1, Véronique Mayeux-Portas, Jawad Khoris, Bertrand de Toffol, Alain Autret, Jean-Pierre Müh, William Camu, Christian Andres.
Abstract
The etiology of amyotrophic lateral sclerosis remains unknown in the majority of cases. Homozygous SMN1 (survival motor neuron) gene deletion causes spinal muscular atrophy, and SMN2 gene deletions are possible risk factors in lower motor neuron disease. We studied SMN1 and SMN2 genes copy numbers in 167 amyotrophic lateral sclerosis patients and in 167 matched controls. We noted that 16% of amyotrophic lateral sclerosis patients had an abnormal copy number of the SMN1 gene (1 or 3 copies), compared with 4% of controls. An abnormal SMN1 gene locus may be a susceptibility factor for amyotrophic lateral sclerosis.Entities:
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Year: 2002 PMID: 11835381 DOI: 10.1002/ana.10104
Source DB: PubMed Journal: Ann Neurol ISSN: 0364-5134 Impact factor: 10.422