Charcot-Marie-Tooth disease, axonal, mitochondrial form, 1
Also known as: CMTMA1
Also known as: CMTMA1
Also known as: CMT2DD, Charcot-Marie-Tooth neuropathy, type 2Dd, Charcot-Marie-tooth disease, axonal, type 2DD
Also known as: CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2EE, CMT2EE, Charcot-Marie-Tooth Neuropathy, Type 2Ee
Also known as: CMT2FF, Charcot-Marie-Tooth neuropathy
Also known as: CMT2GG, CMTDIA, Charcot-Marie-Tooth disease dominant intermediate A, Charcot-Marie-Tooth disease dominant intermediate type A, Charcot-Marie-Tooth disease, dominant intermediate A, Charcot-Marie-Tooth neuropathy dominant intermediate A, Charcot-Marie-Tooth neuropathy, dominant Intermediate a, DI-CMTA, Di-Cmta, autosomal dominant intermediate Charcot-Marie-Tooth disease type A
Also known as: CMT2HH
Also known as: CMT2 with vocal cord paresis, autosomal recessive, Charcot-Marie-Tooth disease, axonal, with vocal cord paresis, autosomal recessive, Charcot-Marie-Tooth disease, type 4A, axonal form, Charcot-Marie-Tooth neuropathy, axonal, with vocal cord paresis, autosomal recessive
Also known as: CMT1G, Charcot-Marie-Tooth disease, demyelinating, type 1G, PMP2-related Charcot-Marie-Tooth disease type 1
Please complete this form to access the requested resource.