Charcot-Marie-Tooth (CMT) disease type 4A, an autosomal recessive neuropathy, arises from mutations in ganglioside-induced differentiation-associated protein 1 (GDAP1). GDAP1 resides in the outer mitochondrial membrane facing the cytosol and is involved in mitochondrial dynamics and function. Its pe...
ORGANISM(S): Homo Sapiens (human)
