W C Koller. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Chromosome AberrationsChromosome DisordersChromosomes, Human, Pair 2/geneticsChromosomes, Human, Pair 3/geneticsGenetic Linkage/geneticsHumansTremor/genetics
Year: 1997 PMID: 9399204 DOI: 10.1002/mds.870120602
Source DB: PubMed Journal: Mov Disord ISSN: 0885-3185 Impact factor: 10.338