Distinct and novel SLC26A4/Pendrin mutations in Chinese and U.S. patients with nonsyndromic hearing loss (Physiological Genomics (2009) 38, (281-290) DOI: 10.1152/physiolgenomics.00047.2009)

P. Dai, A. K. Stewart, F. Chebib, A. Hsu, J. Rozenfeld, D. Huang, D. Kang, V. Lip, H. Fang, H. Shao, X. Liu, F. Yu, H. Yuan, M. Kenna, D. T. Miller, Y. Shen, W. Yang, I. Zelikovic, O. S. Platt, D. HanS. L. Alper, B. L. Wu

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