Article
UBQLN2 in familial amyotrophic lateral sclerosis in The Netherlands.
Neurobiology of aging - 1 Sept 2012
van Doormaal Perry T C, van Rheenen Wouter, van Blitterswijk Marka, Schellevis Raymond D, Schelhaas Helenius J, de Visser Marianne, van der Kooi Anneke J, Veldink Jan H, van den Berg Leonard H
Abstract excerpt
Recently it was discovered that mutations in the UBQLN2 gene were a cause of an X-linked dominant type of familial amyotrophic lateral sclerosis (ALS). We investigated the frequency of mutations in this gene in a cohort of 92 families with ALS in the Netherlands. Eight families were excluded beca...
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