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Abstract
Mesh: See more » Friedreich Ataxia/geneticsGenetic Diseases, InbornHumansHuntington DiseaseOphthalmoplegia/geneticsParkinson Disease/genetics
Year: 1974 PMID: 4274252 PMCID: PMC1633587
Source DB: PubMed Journal: Br Med J ISSN: 0007-1447