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A mutation in PNPT1, encoding mitochondrial-RNA-import protein PNPase, causes hereditary hearing loss
Simon Von Ameln, Geng Wang, Redouane Boulouiz, Mark A. Rutherford, Geoffrey M. Smith, Yun Li, Hans Martin Pogoda, Gudrun Nürnberg, Barbara Stiller, Alexander E. Volk, Guntram Borck, Jason S. Hong, Richard J. Goodyear, Omar Abidi, Peter Nürnberg, Kay Hofmann, Guy P. Richardson, Matthias Hammerschmidt, Tobias Moser, Bernd Wollnik
Research output: Contribution to journal › Article › peer-review
77
Scopus
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