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Article

Genetics of familial ALS and consequences for diagnosis. French ALS Research Group.

Journal of the neurological sciences - 1 Jun 1999

Camu W, Khoris J, Moulard B, Salachas F, Briolotti V, Rouleau G A, Meininger V

Abstract excerpt

Familial amyotrophic lateral sclerosis (fALS) is a well-recognised condition that accounts for almost 10% of all cases of ALS. Most cases are now known to be transmitted by an autosomal dominant trait. When fALS is compared clinically to sporadic ALS, 20% of cases manifest atypical features such as pain, paraesthesia or urgency micturition. Moreover, a disease duration of over 10 years, with very slow...

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Identifiers

PMID: 10448977
DOI: 10.1016/s0022-510x(99)00022-2

Genes

SOD1

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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