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Abstract
Entities: Disease
Mesh: See more » Chromosome MappingChromosomes, Human, Pair 22/geneticsDementia, Vascular/geneticsHumans
Year: 2001 PMID: 11170904 PMCID: PMC1235293 DOI: 10.1086/318180
Source DB: PubMed Journal: Am J Hum Genet ISSN: 0002-9297 Impact factor: 11.025