O.24 Loss of function of MGME1, a novel player in mitochondrial DNA replication, causes a distinct autosomal recessive mitochondrial disorder
Cornelia Kornblum(University of Bonn), Holger Prokisch(Helmholtz Zentrum München), Arcangela Iuso(Helmholtz Zentrum München), Tobias B. Haack(Technical University of Munich), Monica Sciacco(Muscular Dystrophy Association), Dario Ronchi(University of Cambridge), Thomas Klopstock(Ludwig-Maximilians-Universität München), Giacomo P. Comi(University of Milan), Michal Minczuk(MRC Mitochondrial Biology Unit), Gábor Zsurka(University of Bonn), Catarina M. Quinzii(Columbia University Irving Medical Center), Kerstin Hallmann(University Hospital Bonn), Thomas J. Nicholls(Newcastle University), Thomas Wieland(Mannheim Centre for European Social Research), Joanna Rorbach(Karolinska Institutet), Vamsi K. Mootha(Center for Human Genetics), Katharina Danhauser(Helmholtz Zentrum München), Maurizio Moggio(University of Milan), Viktoriya Peeva(University of Bonn), Wolfram S. Kunz(Klinikum Magdeburg), S. DiMauro(Columbia University), Tim M. Strom(Ludwig-Maximilians-Universität München), Sarah E. Calvo(Broad Institute), S. Schoeler, Thomas Meitinger(Helmholtz Zentrum München)
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