Identification of a rare SEPT9 variant in a family with autosomal dominant Charcot-Marie-Tooth disease

Charcot-Marie-Tooth disease (CMT) is one of the most commonly inherited neurological disorders. A growing number of genes, involved in glial and neuronal functions, have been associated with different subtypes...

Source: BMC Medical Genetics - March 2, 2020 Category: Genetics & Stem Cells Authors: Gerrit M. Grosse, Christine Bauer, Bruno Kopp, Christoph Schrader and Alma Osmanovic Tags: Research article Source Type: research