genetics
Last reviewed 01/2018
Charcot-Marie-Tooth is inherited in an autosomal dominant manner.
Charcot-Marie-Tooth-1A is caused by duplication of the peripheral myelin protein gene on chromosome 17.
You are currently on the
UK version of this site. To see content specific to your location,
please choose your country or region.
GPnotebook no longer supports Internet Explorer. To ensure the site functions as intended, please
upgrade your browser. Microsoft is encouraging users to upgrade to its more modern
Edge browser for improved security and functionality.