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Colour vision defects in asymptomatic carriers of the Leber's hereditary optic neuropathy (LHON) mtDNA 11778 mutation from a large Brazilian LHON pedigree: a case-control study.
Quiros PA, Torres RJ, Salomao S, Berezovsky A, Carelli V, Sherman J, Sadun F, De Negri A, Belfort R, Sadun AA. Quiros PA, et al. Among authors: sadun aa, sadun f. Br J Ophthalmol. 2006 Feb;90(2):150-3. doi: 10.1136/bjo.2005.074526. Br J Ophthalmol. 2006. PMID: 16424523 Free PMC article.
Evidence for a novel x-linked modifier locus for leber hereditary optic neuropathy.
Shankar SP, Fingert JH, Carelli V, Valentino ML, King TM, Daiger SP, Salomao SR, Berezovsky A, Belfort R Jr, Braun TA, Sheffield VC, Sadun AA, Stone EM. Shankar SP, et al. Among authors: sadun aa. Ophthalmic Genet. 2008 Mar;29(1):17-24. doi: 10.1080/13816810701867607. Ophthalmic Genet. 2008. PMID: 18363168
364 results