R N Rosenberg. Show Affiliations »
Abstract
Mesh: See more » Fragile X Syndrome/geneticsGene AmplificationHumansMyotonic Dystrophy/complicationsMyotonic Dystrophy/geneticsMyotonic Dystrophy/physiopathology
Year: 1992 PMID: 1407564 DOI: 10.1212/wnl.42.10.1857
Source DB: PubMed Journal: Neurology ISSN: 0028-3878 Impact factor: 9.910