Identification of KLHL41 Mutations Implicates BTB-Kelch-Mediated Ubiquitination as an Alternate Pathway to Myofibrillar Disruption in Nemaline Myopathy

Vandana Gupta(Brigham and Women's Hospital), Alan H. Beggs(Broad Institute), Carina Wallgren‐Pettersson(University of Helsinki), Richard J. N. Allcock(The University of Western Australia), Kathryn N. North(Children's Hospital at Westmead), Sarah A. Sandaradura(The University of Sydney), Masaaki Shiina(Yokohama City University), Michelle A. Farrar(UNSW Sydney), Nigel G. Laing(Harry Perkins Institute of Medical Research), Cynthia Hsu(Boston Children's Hospital), Catherine A. Brownstein(Boston Children's Hospital), Emily J. Todd(The University of Western Australia), Caroline A. Sewry(Great Ormond Street Hospital), Mark R. Davis(University of Oregon), Kyle S. Yau(The University of Western Australia), Kazuhiro Ogata(Yokohama City University), Francesco Muntoni(Great Ormond Street Hospital), Timothy W. Yu(Broad Institute), Ranad Shaheen(King Faisal Specialist Hospital & Research Centre), Ichizo Nishino(National Center of Neurology and Psychiatry), Gianina Ravenscroft(Harry Perkins Institute of Medical Research), Basil T. Darras, Nigel F. Clarke(Newcastle University), Fowzan S. Alkuraya(Alfaisal University), Naomichi Matsumoto(Yokohama City University), Elizabeth M. Thompson(Women's and Children's Hospital), Amal Hashem(King Faisal Specialist Hospital & Research Centre), Nicholas Manton(South Australia Pathology), Lindsay C. Swanson(Boston Children's Hospital), Yukiko Hayashi(Tokyo Medical University)
The American Journal of Human Genetics
November 21, 2013
Cited by 164


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