Gene: [0Xq2/CMTX4] Charcot-Marie-Tooth disease with deafness and mental retardation (Cowchock syndrome); hereditary motor and sensory neuropathy type II, with deafness and mental retardation; [NADMR ]

REF	LIN,LOC "Priest JM &: Genomics, 29, 409-412, 1995
KEY	neu
CLA	unknown, basic
LOC	0X q24-26.1
MIM	MIM: 310490
SYN	NADMR

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Gene: [17p112/PMP22] peripheral myelin protein 22; growth arrest-specific gene 3; Charcot-Marie-Tooth neuropathy 1A (MIM:118220); neuropathy, hereditary, with liability to pressure palsies (MIM:162500); hereditary motor and sensory neuropat