Associated Papers
Genetic spectrum of Charcot-Marie-Tooth disease associated with myelin protein zero gene variants in Japan.
Taniguchi T et al.
Clinical Genetics, 2021
Two novel MPZ mutations in Chinese CMT patients.
Liu L et al.
Journal of the Peripheral Nervous System : Jpns, 2013
Myelin protein zero Arg36Gly mutation with very late onset and rapidly progressive painful neuropathy.
Dacci P et al.
Journal of the Peripheral Nervous System : Jpns, 2012
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