Whole Exome Sequencing and Homozygosity Mapping Identify Mutation in the Cell Polarity Protein GPSM2 as the Cause of Nonsyndromic Hearing Loss DFNB82
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Open Access
- 17 June 2010
- journal article
- other
- Published by Elsevier in American Journal of Human Genetics
- Vol. 87 (1), 90-94
- https://doi.org/10.1016/j.ajhg.2010.05.010
Abstract
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