John Kamholz, Michael E Shy. Show Affiliations »
Abstract
Entities: Disease Gene Mutation
Mesh: See more » Amino Acid SequenceAmino Acid SubstitutionCharcot-Marie-Tooth Disease/geneticsCodon/geneticsHumansMutation, MissenseMyelin P0 Protein/chemistryMyelin P0 Protein/genetics
Substances: See more » CodonMyelin P0 Protein
Year: 2004 PMID: 15249646 DOI: 10.1212/wnl.63.1.194
Source DB: PubMed Journal: Neurology ISSN: 0028-3878 Impact factor: 9.910