Identification of a rare SEPT9 variant in a family with autosomal dominant Charcot-Marie-Tooth disease | BMC Medical Genetics | Full Text

Identification of a rare SEPT9 variant in a family with autosomal dominant Charcot-Marie-Tooth disease | BMC Medical Genetics | Full Text

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...

Authors:Gerrit M. Grosse, Christine Bauer, Bruno Kopp, Christoph Schrader and Alma Osmanovic

Citation:BMC Medical Genetics 2020 21:45

Content type:Research article

Published on: 2 March 2020

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