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Multiphasic analysis of whole exome sequencing data identifies a novel mutation of ACTG1 in a nonsyndromic hearing loss family

Gibeom Park, Jungsoo Gim, Ah Reum Kim, Kyu-Hee Han, Hyo-Sang Kim, Seung-Ha Oh, Taesung Park, Woong-Yang Park* and Byung Yoon Choi*

BMC Genomics 2013, 14:191  doi:10.1186/1471-2164-14-191

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