Whole Exome Sequencing and Homozygosity Mapping Identify Mutation in the Cell Polarity Protein GPSM2 as the Cause of Nonsyndromic Hearing Loss DFNB82 by unknow
Author:unknow , Date: December 2, 2022
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Author:unknow
Format: pdf
Tags: The American Journal of Human Genetics, 87 (2010) 90-94. doi:10.1016/j.ajhg.2010.05.010
Publisher: The American Society of Human Genetics
Published: 0101-01-01T00:00:00+00:00
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