Exome sequencing identifies ACAD9 mutations as a cause of complex I deficiency
Haack, Tobias B, Danhauser, Katharina, Haberberger, Birgit, Hoser, Jonathan, Strecker, Valentina, Boehm, Detlef, Uziel, Graziella, Lamantea, Eleonora, Invernizzi, Federica, Poulton, JoannaVolume:
42
Year:
2010
Language:
english
Pages:
4
DOI:
10.1038/ng.706
File:
PDF, 478 KB
english, 2010