F C ROSE, A I FRIEDMANN. Show Affiliations »
Abstract
Entities: Disease
Keywords: CHROMOSOMES; OPTIC ATROPHY
Mesh： See more » ChromosomesHumansLeber Congenital AmaurosisOptic AtrophyOptic Atrophy, Hereditary, Leber
Year: 1964 PMID： 14234105 PMCID： PMC1012757 DOI： 10.1136/jmg.1.2.110
Source DB: PubMed Journal: J Med Genet ISSN： 0022-2593 Impact factor: 6.318