Recurrent De Novo Dominant Mutations in SLC25A4 Cause Severe Early-Onset Mitochondrial Disease and Loss of Mitochondrial DNA Copy Number
Kyle Thompson(Wellcome Centre for Mitochondrial Research), Robert W. Taylor(Royal Victoria Infirmary), Alon Haham(Tel Aviv Sourasky Medical Center), Pirjo Isohanni(University of Helsinki), Katrin Õunap(Tartu University Hospital), Nitay Fraenkel(Alyn Hospital), Inês A. Barbosa(King's College London), Ileana Ferrero(University of Parma), Orly Elpeleg(Hadassah Medical Center), Michael A. Simpson(Guy's Hospital), Ann Saada(Jerusalem College of Technology), Homa Majd(University of California, San Francisco), Robert McFarland(Wellcome Centre for Mitochondrial Research), Simon Jones(Manchester Academic Health Science Centre), Charlotte L. Alston(Wellcome Centre for Mitochondrial Research), Anu Suomalainen(University of Helsinki), Edmund R.S. Kunji(MRC Mitochondrial Biology Unit), Cristina Dallabona(University of Parma), Roshni Vara(Evelina London Children's Healthcare), Richard J. Rodenburg(Amalia Kinderziekenhuis), Sanna Puusepp(Tartu University Hospital), Martin King(MRC Mitochondrial Biology Unit), Penelope E. Bonnen(Baylor College of Medicine), Tiziana Lodi(University of Parma), Aviva Fattal‐Valevski(Tel Aviv University), Charu Deshpande(Guy's Hospital), Langping He(Wellcome Centre for Mitochondrial Research), Karit Reinson(Tartu University Hospital)
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