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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
  1. Correspondence to: P A Quiros MD, Doheny Eye Institute, 1450 San Pablo Street, Los Angeles, CA 90033, USA; pquiros{at}usc.edu
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Quiros PA, Torres RJ, Salomao S, et al
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

Publication history

  • Accepted September 2, 2005
  • First published January 19, 2006.
Online issue publication 
March 22, 2016

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