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 (Q36373027)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | 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 |
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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 (English)
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P A Quiros
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R J Torres
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S Salomao
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A Berezovsky
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V Carelli
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J Sherman
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F Sadun
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A De Negri
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R Belfort
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A A Sadun
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1 February 2006
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150-153
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