Mutations in the GDAP1 mitochondrial outer membrane gene cause Charcot-Marie-Tooth
(CMT) neuropathy. Reduction or absence of GDAP1 has been associated with abnormal …

Ganglioside-induced differentiation associated protein 1 (GDAP1) gene encodes a protein
of the mitochondrial outer membrane and of the mitochondrial membrane contacts with the …

Mutations in GDAP1, which encodes protein located in the mitochondrial outer membrane,
cause axonal recessive (AR-CMT2), axonal dominant (CMT2K) and demyelinating …

Mutations in the mitochondrial protein GDAP1 are the cause of Charcot‐Marie‐Tooth type
4A disease (CMT4A), a severe form of peripheral neuropathy associated with either …

The pathology of Charcot-Marie-Tooth (CMT), a disease arising from mutations in different
genes, has been associated with an impairment of mitochondrial dynamics and axonal …

ABSTRACT GDAP1 pathogenic variants cause Charcot-Marie-Tooth (CMT) disease, the
most common hereditary motor and sensory neuropathy. CMT-GDAP1 can be axonal or …

Mutations in the ganglioside-induced differentiation associated protein 1 (GDAP1) gene
have been associated with demyelinating and axonal forms of Charcot-Marie-Tooth (CMT) …

The ganglioside-induced differentiation-associated protein 1 (GDAP1) is a mitochondrial
fission factor and mutations in GDAP1 cause Charcot–Marie–Tooth disease. We found that …

One of the genes involved in Charcot–Marie–Tooth (CMT) disease, an inherited peripheral
neuropathy, is GDAP1. In this work, we show that there is a true ortholog of this gene in …

Mutations in GDAP1 lead to recessively or dominantly inherited peripheral neuropathies
(Charcot–Marie–Tooth disease, CMT), indicating that GDAP1 is essential for the viability of …