A Founder Mutation in PET100 Causes Isolated Complex IV Deficiency in Lebanese Individuals with Leigh Syndrome
Sze Chern Lim(Victorian Clinical Genetics Services), David R. Thorburn(Royal Children's Hospital), David A. Stroud(Monash University), Matthew McKenzie(Monash Institute of Medical Research), Luke C. Gandolfo(The University of Melbourne), Heidi Peters(Royal Children's Hospital), Katherine R. Smith(Murdoch Children's Research Institute), David Mowat(UNSW Sydney), John Christodoulou(The University of Melbourne), Alison G. Compton(Royal Children's Hospital), Justine E. Marum(Victorian Clinical Genetics Services), Melanie Bahlo(Walter and Eliza Hall Institute of Medical Research), Michael T. Ryan(Australian Regenerative Medicine Institute), Elena J. Tucker(The University of Melbourne), Garry K. Brown(Churchill Hospital), Bridget Wilcken(The University of Sydney), Peter G. Procopis(The University of Sydney), Ayan Dasvarma(Royal Children's Hospital)
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