Whole Exome Sequencing and Homozygosity Mapping Identify Mutation in the Cell Polarity Protein GPSM2 as the Cause of Nonsyndromic Hearing Loss DFNB82

2010287 citationsJournal Articlebronze Open Access

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Good health and well-being

Published in: The American Journal of Human Genetics

Volume 87, Issue 1, pp. 90-94

Field-Weighted Citation Impact: 20.01