Exome sequencing identifies ACAD9 mutations as a cause of complex I deficiency
Tobias B. Haack(Helmholtz Zentrum München), Katharina Danhauser(Technical University of Munich), Birgit Haberberger(Technical University of Munich), Jonathan Hoser(Institute of Bioinformatics and Systems Biology), Valentina Strecker(Goethe University Frankfurt), Detlef Boehm(CeGaT (Germany)), Graziella Uziel(Istituti di Ricovero e Cura a Carattere Scientifico), Eleonora Lamantea(Fondazione IRCCS Istituto Neurologico Carlo Besta), Federica Invernizzi(Fondazione IRCCS Istituto Neurologico Carlo Besta), Joanna Poulton(University of Oxford), Boris Rolinski(München Klinik), Arcangela Iuso(Helmholtz Zentrum München), Saskia Biskup(CeGaT (Germany)), Thorsten Schmidt(Helmholtz Zentrum München), Hans‐Werner Mewes(Institute of Bioinformatics and Systems Biology), Ilka Wittig(Goethe University Frankfurt), Thomas Meitinger(Helmholtz Zentrum München), Massimo Zeviani(Fondazione IRCCS Istituto Neurologico Carlo Besta), Holger Prokisch(Helmholtz Zentrum München)
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