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Perrault syndrome is caused by recessive mutations in CLPP, encoding a mitochondrial ATP-dependent chambered protease

scientific article published on 28 March 2013

Author/s

author: Graeme Black, Mary-Claire King, Neil Billington, Robert J. Morell, Jill E. Urquhart, Kwanghyuk Lee, Tom Walsh, Neil A. Hanley, William G. Newman, Peter E. Clayton, University of Washington Center for Mendelian Genomics, Suzanne M. Leal

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Work details

Publication date
March 28, 2013
- -
Language
English

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