| Literature DB >> 14076016 |
Abstract
Keywords: GENETICS, HUMAN; GLYCOGENOSIS; MUSCULAR DISEASES; MUSCULAR DYSTROPHY; MYOGLOBINURIA; MYOTONIA ATROPHICA; MYOTONIA CONGENITA; PARALYSIS, FAMILIAL PERIODIC; REVIEW
Mesh:
Year: 1963 PMID: 14076016 DOI: 10.1016/0002-9343(63)90134-7
Source DB: PubMed Journal: Am J Med ISSN: 0002-9343 Impact factor: 4.965