Hereditary neuropathy with liability to pressure palsies (HNPP). For current stage of knowledge see reference 1. 601097, 159440, 304040, 608507, 129010, 603795 ...
A 1.4-Mb tandem duplication, including the gene for peripheral myelin protein 22 (PMP22) in chromosome 17p11.2-12 is responsible for 70% of the cases of the demyelinating type 1 of Charcot-Marie-Tooth ...
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