A mutation in the human heme A:farnesyltransferase gene (COX10 ) causes cytochrome c oxidase deficiency (Q22253915)
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Language | Label | Description | Also known as |
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English | A mutation in the human heme A:farnesyltransferase gene (COX10 ) causes cytochrome c oxidase deficiency |
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A mutation in the human heme A:farnesyltransferase gene (COX10 ) causes cytochrome c oxidase deficiency (English)
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I Valnot
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J C von Kleist-Retzow
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A Barrientos
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M Gorbatyuk
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J W Taanman
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B Mehaye
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P Rustin
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A Tzagoloff
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A Rötig
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1 May 2000
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9
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8
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1245-9
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