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(Charles Darwin University), 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(King's College London), Ann Saada(Shaare Zedek Medical Center), Homa Majd(University of Cambridge), Robert McFarland(Wellcome Centre for Mitochondrial Research), Simon Jones(Manchester University NHS Foundation Trust), Charlotte L. Alston(Newcastle upon Tyne Hospitals NHS Foundation Trust), Anu Suomalainen(University of Helsinki), Edmund R.S. Kunji(University of Cambridge), Cristina Dallabona(University of Parma), Roshni Vara(Evelina London Children's Healthcare), Richard J. Rodenburg(Radboud University Nijmegen), Sanna Puusepp(Tartu University Hospital), Martin King(University of Cambridge), 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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