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Published in 2021 at "Biomolecules"
DOI: 10.3390/biom11040601
Abstract: Charcot–Marie–Tooth (CMT) type 1 disease is the most common human hereditary demyelinating neuropathy. Mutations in pmp22 cause about 70% of all CMT1. Trembler-J (TrJ/+) mice are an animal model of CMT1E, having the same spontaneous…
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Keywords:
anxiety;
anxiety tests;
peripheral neuropathy;
pmp22 ... See more keywords