Novel mutation of the myelin P0 gene in a CMT1B family
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
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4. Structure and Chromosomal Localization of the Gene Encoding the Human Myelin Protein Zero (MPZ)
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3. The cytoplasmic tail of myelin protein zero induces morphological changes in lipid membranes;2024-03-22
4. Structural context of homomeric interactions in the lg domain of the MPZ (P0) myelin adhesion protein and relation to Charcot-Marie-Tooth disease phenotype variants;2023-03-19
5. Genetic and clinical spectrums in Korean Charcot‐Marie‐Tooth disease patients with myelin protein zero mutations;Molecular Genetics & Genomic Medicine;2021-04-06
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