Biallelic Mutations in NDUFA6 Establish Its Role in Early-Onset Isolated Mitochondrial Complex I Deficiency.

Journal: American Journal of Human Genetics

Published: 2018-09-14

DOI: 10.1016/j.ajhg.2018.08.013

Affiliations: 26

Authors: 31

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Institutions FC
Salzburger Landeskliniken (SALK), Austria 0.10
Division of Pediatric Neurology, University of Göttingen, Germany 0.10
Wellcome Trust Centre for Mitochondrial Research, Newcastle University, United Kingdom (UK) 0.08
Institute of Neuroscience (ION), Newcastle University, United Kingdom (UK) 0.08
Institute of Physiology, CAS, Czech Republic 0.06
TUM-HMGU Institute of Human Genetics (IHG), Germany 0.06
Faculty of Medical Science (FB16), GU, Germany 0.04
Cambridge University Hospitals NHS Foundation Trust, United Kingdom (UK) 0.04
Academic Department of Medical Genetics, University of Cambridge, United Kingdom (UK) 0.03
Cambridge Institute for Medical Research (CIMR), University of Cambridge, United Kingdom (UK) 0.03
Brighton and Sussex University Hospitals NHS Trust (BSUH), United Kingdom (UK) 0.03
Oxford Nuffield Department of Women's and Reproductive Health, United Kingdom (UK) 0.03
Cologne Center for Genomics (CCG), UoC, Germany 0.03
Drammen Sykehus, Norway 0.03
NIHR Oxford Biomedical Research Centre (OxBRC), United Kingdom (UK) 0.03
Evelina London Children’s Hospital, Guy's and St Thomas' NHS Foundation Trust, United Kingdom (UK) 0.03
Department of Biochemistry and Molecular Biology, Monash University, Australia 0.03
Monash Biomedicine Discovery Institute (BDI), Monash University, Australia 0.03
NIHR BioResource, United Kingdom (UK) 0.02
Churchill Hospital, United Kingdom (UK) 0.02
Oxford Medical Genetics Laboratories, OUH, United Kingdom (UK) 0.02
Oxford Nuffield Department of Surgical Sciences (NDS), United Kingdom (UK) 0.02
Oxford University Hospitals NHS Trust (OUH), United Kingdom (UK) 0.02
DZHK Partner Site Rhine-Main, Germany 0.01
Cluster of Excellence - Macromolecular Complexes (CEF-MC), GU, Germany 0.01

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