J P Fryns, E Smeets. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Abnormalities, Multiple/physiopathologyCataplexy/complicationsHumansMaleNeuromuscular Diseases/physiopathologySyndrome
Year: 1998 PMID: 9719387 PMCID: PMC1051409 DOI: 10.1136/jmg.35.8.702
Source DB: PubMed Journal: J Med Genet ISSN: 0022-2593 Impact factor: 6.318