WGS and RNA Studies Diagnose Noncoding <i>DMD</i> Variants in Males With High Creatine Kinase

Leigh B. Waddell(The University of Sydney), Sandra T. Cooper(Children's Medical Research Institute), Michel Tchan(Westmead Hospital), Emily C. Oates(The University of Sydney), Rebecca Gooding(Queen Elizabeth II Medical Centre), Taru Tukiainen(Broad Institute), Amanda Charlton(The University of Sydney), Sarah A. Sandaradura(Children's Hospital at Westmead), Beryl B. Cummings(Rapt Therapeutics (United States)), Monkol Lek(Massachusetts General Hospital), Alan Ma(The University of Sydney), Michelle A. Farrar(Sydney Children's Hospital), Diane Kenwright(Children's Hospital at Westmead), Kristi Jones(South Australia Pathology), David Mowat(UNSW Sydney), Simon Sadedin(Murdoch Children's Research Institute), Elise Valkanas(Broad Institute), Adam Bournazos(The University of Sydney), Mark R. Davis(Pathwest Laboratory Medicine), Susan Arbuckle(Gazi University), Fathimath Faiz(Queen Elizabeth II Medical Centre), Jamie L. Marshall(Solidus Biosciences (United States)), Ben Weisburd(MACOM (United States)), Min‐Xia Wang(UNSW Sydney), Nigel F. Clarke(Newcastle University), Samantha J. Bryen(Garvan Institute of Medical Research), Nicole Graf(Children's Hospital at Westmead), Gina O’Grady(Starship Children's Health), Katherine Neas(Northwell Health), Himanshu Joshi(Children's Hospital at Westmead), Charles Chan(Children's Hospital at Westmead), Daniel G. MacArthur(Garvan Institute of Medical Research), Hugo Sampaio(Sydney Children’s Hospitals Network), Frances J. Evesson(Harvard University)
Neurology Genetics
January 30, 2021
Cited by 31


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