Biallelic Mutations in TMEM126B Cause Severe Complex I Deficiency with a Variable Clinical Phenotype
Charlotte L. Alston(Newcastle upon Tyne Hospitals NHS Foundation Trust), Robert W. Taylor(Wellcome Centre for Mitochondrial Research), Ilka Wittig(Goethe University Frankfurt), Luke E. Formosa(Australian Regenerative Medicine Institute), Tobias B. Haack(Technical University of Munich), Sara Seneca(Vrije Universiteit Brussel), David Cassiman, Valentina Strecker(Goethe University Frankfurt), Ewa Pronicka(Children's Memorial Health Institute), Monika Oláhová(University of Helsinki), Rafał Płoski(Medical University of Warsaw), Boél De Paepe(Ghent University Hospital), David R. Thorburn(Royal Children's Hospital), Alison G. Compton(Royal Children's Hospital), Arnaud Vanlander(Ghent University Hospital), Holger Prokisch(Helmholtz Zentrum München), Elżbieta Ciara(Children's Memorial Health Institute), Joél Smet(Ghent University Hospital), Melanie Bahlo(Walter and Eliza Hall Institute of Medical Research), Peter Diakumis(The University of Melbourne), Ronald G. Haller(The University of Texas Southwestern Medical Center), John W. Yarham(Wellcome Centre for Mitochondrial Research), René G. Feichtinger(Paracelsus Medical University), Dariusz Rokicki(Children's Memorial Health Institute), Johannes A. Mayr(Paracelsus Medical University), Johan L.K. Van Hove(Children's Hospital Colorado), Michael T. Ryan(Australian Regenerative Medicine Institute), Rudy Van Coster, Nadine Romain(Texas Health Dallas), Langping He(Wellcome Centre for Mitochondrial Research), Katrien Stouffs(Vrije Universiteit Brussel)
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