L N Went, G W Bruyn. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » AdultChildFemaleHumansMaleNeurologic Manifestations/geneticsOptic Atrophy/complicationsOptic Atrophy/geneticsPedigreeSex Chromosomes
Year: 1966 PMID: 5987544
Source DB: PubMed Journal: J Genet Hum ISSN: 0021-7743