Биология и медицина

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 ]

Ссылки:

• 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