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Published in 2019 at "Human Molecular Genetics"
DOI: 10.1093/hmg/ddy336
Abstract: Abstract Protein zero (P0) is the major structural protein in peripheral myelin, and mutations in the Myelin Protein Zero (Mpz) gene produce wide‐ranging hereditary neuropathy phenotypes. To gain insight in the mechanisms underlying a particularly…
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Keywords:
protein;
abnormal function;
hypomyelination;
gain abnormal ... See more keywords