A E Emery, J N Walton. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » HumansMuscular Dystrophies/geneticsMyotonia/geneticsMyotonia Congenita/geneticsMyotonic Dystrophy/genetics
Year: 1967 PMID: 4903571 DOI: 10.1016/b978-1-4831-6757-2.50008-7
Source DB: PubMed Journal: Prog Med Genet ISSN: 0079-6441