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
33179255 (PubMed )
Supplement: CGE-99-359-s001.docx
Congenital hypomyelinating neuropathy due to a novel MPZ mutation.
Sevilla T et al.
Journal of the Peripheral Nervous System : Jpns, 2011
Novel MPZ mutations and congenital hypomyelinating neuropathy.
McMillan HJ et al.
Neuromuscular Disorders : Nmd, 2010
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