Associated Papers
Clinical characterization and genetic analysis of Korean patients with X-linked Charcot-Marie-Tooth disease type 1.
Hong YB et al.
Journal of the Peripheral Nervous System : Jpns, 2017
Mutations in noncoding regions of GJB1 are a major cause of X-linked CMT.
Tomaselli PJ et al.
Neurology, 2017
28283593 (PubMed )
Supplement: supp_WNL.0000000000003819_Table_e-2.pdf
Charcot-Marie-Tooth disease: genetic and clinical spectrum in a Spanish clinical series.
Sivera R et al.
Neurology, 2013
Mutation analysis of the PMP22, MPZ, EGR2, LITAF, and GJB1 genes in Korean patients with Charcot-Marie-Tooth neuropathy type 1.
Park HK et al.
Clinical Genetics, 2006
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