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Exome sequencing identifies ACAD9 mutations as a cause of complex I deficiency

✍ Scribed by Haack, Tobias B; Danhauser, Katharina; Haberberger, Birgit; Hoser, Jonathan; Strecker, Valentina; Boehm, Detlef; Uziel, Graziella; Lamantea, Eleonora; Invernizzi, Federica; Poulton, Joanna

Book ID: 109914679
Publisher: Nature Publishing Group
Year: 2010
Tongue: English
Weight: 478 KB
Volume: 42
Category: Article
ISSN: 1061-4036
DOI: 10.1038/ng.706

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