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 P.A.; Torres R.J.; Salomao S.; Berezovsky A.; Carelli V.; Sherman J.; Sadun F.; De Negri A.; Belfort R.; Sadun A.A.. - In: BRITISH JOURNAL OF OPHTHALMOLOGY. - ISSN 0007-1161. - STAMPA. - 90:(2006), pp. 150-153. [10.1136/bjo.2005.074526]
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.
CARELLI, VALERIO;
2006
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