A systematic mutation screen of 10 nuclear and 25 mitochondrial candidate genes in 21 patients with cytochrome c oxidase (COX) deficiency shows tRNA(Ser)(UCN) mutations in a subgroup with syndromal encephalopathy (Q33681493)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | A systematic mutation screen of 10 nuclear and 25 mitochondrial candidate genes in 21 patients with cytochrome c oxidase (COX) deficiency shows tRNA(Ser)(UCN) mutations in a subgroup with syndromal encephalopathy |
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A systematic mutation screen of 10 nuclear and 25 mitochondrial candidate genes in 21 patients with cytochrome c oxidase (COX) deficiency shows tRNA(Ser)(UCN) mutations in a subgroup with syndromal encephalopathy (English)
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Jaksch M
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Hofmann S
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Kleinle S
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Liechti-Gallati S
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Pongratz DE
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Müller-Höcker J
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Jedele KB
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Gerbitz KD
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1 November 1998
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895-900
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