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Characterization of the human complex I NDUFB7 and 17.2-kDa cDNAs and mutational analysis of 19 genes of the HP fraction in complex I-deficient-patients

✍ Scribed by Ralf Triepels; Jan Smeitink; Jan Loeffen; Roel Smeets; Frans Trijbels; Lambert van den Heuvel

No coin nor oath required. For personal study only.

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Molecular characterization and mutationa

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Mapping to 1q23 of the human gene (NDUFS

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Sequence of exons and the flanking regio

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Crigler-Najjar syndrome, type I is a heterogeneous