PMP22 related neuropathies: Charcot-Marie-Tooth disease type 1A and Hereditary Neuropathy with liability to Pressure Palsies
Authors
Keywords
Peripheral myelin protein 22 (PMP22), Charcot-Marie-Tooth disease type 1A (CMT1A), Hereditary Motor and Sensory Neuropathy type Ia (HMSN Ia), Hereditary Neuropathy with liability to Pressure Palsies (HNPP), Demyelinating, Clinical description, Genetic counselling
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