A double mutation (G11778A and G12192A) in mitochondrial DNA associated with Leber's hereditary optic neuropathy and cardiomyopathy. (Q51950786)
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scientific article published in January 2003
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | A double mutation (G11778A and G12192A) in mitochondrial DNA associated with Leber's hereditary optic neuropathy and cardiomyopathy. |
scientific article published in January 2003 |
Statements
A double mutation (G11778A and G12192A) in mitochondrial DNA associated with Leber's hereditary optic neuropathy and cardiomyopathy. (English)
1 reference
Masakazu Mimaki
1 reference
Akemi Ikota
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Aya Sato
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Hirofumi Komaki
1 reference
Jun Akanuma
1 reference
Ikuya Nonaka
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Yu-ichi Goto
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1 January 2003
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48
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1
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47-50
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Identifiers
1 reference