Mitochondrial mutation commonly associated with Leber's hereditary optic neuropathy observed in a patient with Wolfram syndrome (DIDMOAD) (Q33673890)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Mitochondrial mutation commonly associated with Leber's hereditary optic neuropathy observed in a patient with Wolfram syndrome (DIDMOAD) |
scientific article |
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Mitochondrial mutation commonly associated with Leber's hereditary optic neuropathy observed in a patient with Wolfram syndrome (DIDMOAD) (English)
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Pilz D
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Quarrell OW
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Jones EW
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1 April 1994
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328-330
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