A Bronner, J P Gerhard, M Collard, S Malamet. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » AdolescentFemaleHumansMaleNerve DegenerationNervous System Diseases/geneticsOptic Atrophy/geneticsSyndrome
Year: 1979 PMID: 472584
Source DB: PubMed Journal: Rev Otoneuroophtalmol ISSN: 0035-2497