OPA3 gene mutations responsible for autosomal dominant optic atrophy and cataract. Issue 9 (1st September 2004)

• Record Type: Journal Article
• Authors: Reynier, P; Amati-Bonneau, P; Verny, C; Olichon, A; Simard, G; Guichet, A; Bonnemains, C; Malecaze, F; Malinge, M C; Pelletier, J B; Calvas, P; Dollfus, H; Belenguer, P; Malthièry, Y; Lenaers, G; Bonneau, D
• Is Part Of: Journal of medical genetics. Volume 41:Issue 9(2004)
• Page Start: e110
• Page End: e110
• Publication Date: 2004-09-01
• Subjects: ADOA, autosomal dominant optic atrophy -- ADOAC, autosomal dominant optic atrophy and cataract -- AROA, autosomal recessive optic atrophy -- LHON, Leber's hereditary optic neuropathy -- MGA, 3-methylglutaconic aciduria -- OPA1, optic atrophy 1 -- OPA3, optic atrophy 3 -- XLAO, X linked optic atrophy; OPA3 -- dominant optic atrophy -- cataract; Medical genetics -- Periodicals; 616.042
• DOI: 10.1136/jmg.2003.016576
• Languages: English
• ISSNs: 1468-6244