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

AIMS: To determine if asymptomatic carriers from a previously identified large pedigree of the Leber's hereditary optic neuropathy (LHON) 11778 mtDNA mutation have colour vision deficits. METHODS: As part of a comprehensive analysis of over 200 members of a large Brazilian LHON pedigree spannin...

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Bibliografiset tiedot
Päätekijät: Quiros, P A, Torres, R J, Salomao, S, Berezovsky, A, Carelli, V, Sherman, J, Sadun, F, De Negri, A, Belfort, R, Sadun, A A
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BMJ Group 2006
Aiheet:
Clinical Science - Scientific Report
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC1860163/
https://ncbi.nlm.nih.gov/pubmed/16424523
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bjo.2005.074526
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