Literature DB >> 14676054

Mutation screening of the ALS2 gene in sporadic and familial amyotrophic lateral sclerosis.

Collette K Hand1, Rebecca S Devon, Francois Gros-Louis, Daniel Rochefort, Jawad Khoris, Vincent Meininger, Jean-Pierre Bouchard, William Camu, Michael R Hayden, Guy A Rouleau.   

Abstract

BACKGROUND: Mutations in the ALS2 gene cause juvenile-onset autosomal recessive amyotrophic lateral sclerosis (ALS) and hereditary spastic paraplegia.
OBJECTIVE: To assess the role of ALS2 among more common forms of ALS.
METHODS: DNA from 95 unrelated familial, 95 unrelated sporadic, and 11 early-onset ALS patients was screened for mutations in ALS2 by denaturing high-performance liquid chromatography and direct sequencing of polymerase chain reaction-amplified fragments. Each variant identified was also analyzed among control subjects. All 34 exons of ALS2 plus the 5' and 3' untranslated region were screened.
RESULTS: We detected 23 novel sequence variants; however, none is disease-associated.
CONCLUSION: Mutations of ALS2 are not a common cause of ALS.

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Year:  2003        PMID: 14676054     DOI: 10.1001/archneur.60.12.1768

Source DB:  PubMed          Journal:  Arch Neurol        ISSN: 0003-9942


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