Perrault Syndrome Is Caused by Recessive Mutations in CLPP, Encoding a Mitochondrial ATP-Dependent Chambered Protease
- 4 April 2013
- journal article
- case report
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 92 (4), 605-613
- https://doi.org/10.1016/j.ajhg.2013.02.013
Abstract
No abstract availableKeywords
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