Charcot-Marie-Tooth disease axonal type 2T

A Charcot-Marie-Tooth disease type 2 that has material basis in homozygous or compound heterozygous mutation in the MME gene on chromosome 3q25.

Also known as: CMT2T, Charcot-Marie-Tooth disease, axonal, type 2T, DNAJB2-related CMT2, AR-CMT2T, Charcot-Marie-Tooth disease, axonal, autosomal recessive, type 2T, Charcot-Marie-Tooth neuropathy, type 2T, DNAJB2-related Charcot-Marie-Tooth disease type 2, autosomal recessive axonal Charcot-Marie-Tooth disease type 2T

9 clinical trials for this condition and its sub-types, 0 tagged with Charcot-Marie-Tooth disease axonal type 2T itself.