Exome sequencing identifies ACAD9 mutations as a cause of complex I deficiency.
Haack TB; Danhauser K; Haberberger B; Hoser J; Strecker V; Boehm D; Uziel G; Lamantea E; Invernizzi F; Poulton J; Rolinski B; Iuso A; Biskup S; Schmidt T; Mewes HW; Wittig I; Meitinger T; Zeviani M; Prokisch H; Nature Genetics, 2010, vol. 42, issue 12, p 1131, ISSN 15461718. ISBN 15461718.

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