Results
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2641.
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2642.
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2643.
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2644.
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2645.
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2646.
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2647.
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2648.
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2649.
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2650.
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2651.
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2652.
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2653.
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2654.
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2655.
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2656.
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2657.
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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. [electronic resource] by
- Quiros, P A
- Torres, R J
- Salomao, S
- Berezovsky, A
- Carelli, V
- Sherman, J
- Sadun, F
- De Negri, A
- Belfort, R
- Sadun, A A
Producer: 20060223
In:
The British journal of ophthalmology vol. 90
Availability: No items available.
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2658.
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2659.
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2660.
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