Use of transmitochondrial cybrids to assign a complex I defect to the mitochondrial DNA-encoded NADH dehydrogenase subunit 6 gene mutation at nucleotide pair 14459 that causes Leber hereditary optic neuropathy and dystonia

• JUN AS

収録刊行物

• Mol Cell Biol

  Mol Cell Biol 16 771-777, 1996

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• CRID: 1571417126676128000
• NII論文ID: 80008790434
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