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Perrault Syndrome Is Caused by Recessive Mutations in CLPP, Encoding a Mitochondrial ATP-Dependent Chambered Protease

Emma M. Jenkinson, Atteeq U. Rehman, Tom Walsh, Jill Clayton‐Smith, Kwanghyuk Lee, Robert J. Morell, Meghan C. Drummond, Shaheen N. Khan, Muhammad Asif Naeem, Bushra Rauf, Neil Billington, Julie M. Schultz, Jill Urquhart, Ming K. Lee, Andrew Berry, Neil A. Hanley, Sarju Mehta, Deirdre Cilliers, Peter Clayton, Helen Kingston, Miriam J. Smith, Thomas T. Warner, Graeme C. Black, Dorothy Trump, J.R. Davis, Wasim Ahmad, Suzanne M. Leal, Sheikh Riazuddin, Mary‐Claire King, Thomas B. Friedman, William G. Newman

The American Journal of Human Genetics, 2013

University of Manchester, Manchester Academic Health Science Centre, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, University of Washington Medical Center, Baylor College of Medicine, Centre of Excellence in Molecular Biology, University of the Punjab, National Heart Lung and Blood Institute, Addenbrooke's Hospital, Churchill Hospital, University College London, Quaid-i-Azam University, University of Health Sciences Lahore, Allama Iqbal Medical College, Jinnah Postgraduate Medical Center

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