A mitochondrial mutation at nt 9101 in the ATP synthase 6 gene associated with deficient oxidative phosphorylation in a family with Leber hereditary optic neuroretinopathy. (Q42950908)
scientific article published on May 1995
Language:
Current Data About A mitochondrial mutation at nt 9101 in the ATP synthase 6 gene associated with deficient oxidative phosphorylation in a family with Leber hereditary optic neuroretinopathy.
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(P1476) "A mitochondrial mutation at nt 9101 in the ATP synthase 6 gene associated with deficient oxidative phosphorylation in a family with Leber hereditary optic neuroretinopathy" (language: en)
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(P2093) T Lamminen
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A Majander
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V Juvonen
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M Wikström
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P Aula
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E Nikoskelainen
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M L Savontous
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other details
description scientific article published on May 1995

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