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Clin Genet. 2011 Jan;79(1):44-5. doi: 10.1111/j.1399-0004.2010.01556_1.x. Epub 2010 Oct 12.

Deleterious mutation in GPSM2 identified as cause for nonsyndromic deafness.

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  • Centre for Molecular Medicine and Therapeutics, Child and Family Research Institute, 950 West 28th Avenue, Vancouver, BC, Canada. jschulze@cmmt.ubc.ca

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PMID:
21029073
[PubMed]

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