B Stanescu, J Michiels, G Lyon. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » AdolescentAdultCerebellar Ataxia/geneticsElectroretinographyHumansLaurence-Moon Syndrome/geneticsMyotonic Dystrophy/geneticsNeuronal Ceroid-Lipofuscinoses/geneticsPhenotypeRetinal Degeneration/genetics
Year: 1982 PMID: 7171760
Source DB: PubMed Journal: Birth Defects Orig Artic Ser ISSN: 0547-6844