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. Han; S. L. Alper; B. L. Wu

doi:10.1152/physiolgenomics.zh7-3421-corr.2010

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

Nephrology and Hypertension (Internal Med)

Research output: Contribution to journal › Comment/debate › peer-review

1 Scopus citations

Original language	English (US)
Pages (from-to)	216
Number of pages	1
Journal	Physiological Genomics
Volume	40
Issue number	3
DOIs	https://doi.org/10.1152/physiolgenomics.zh7-3421-corr.2010
State	Published - Feb 2010

ASJC Scopus subject areas

Physiology
Genetics

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Dai, P., Stewart, A. K., Chebib, F., Hsu, A., Rozenfeld, J., Huang, D., Kang, D., Lip, V., Fang, H., Shao, H., Liu, X., Yu, F., Yuan, H., Kenna, M., Miller, D. T., Shen, Y., Yang, W., Zelikovic, I., Platt, O. S., ... Wu, B. L. (2010). 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). Physiological Genomics, 40(3), 216. https://doi.org/10.1152/physiolgenomics.zh7-3421-corr.2010

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). / Dai, P.; Stewart, A. K.; Chebib, F. et al.
In: Physiological Genomics, Vol. 40, No. 3, 02.2010, p. 216.

Research output: Contribution to journal › Comment/debate › peer-review

Dai, P, Stewart, AK, Chebib, F, Hsu, A, Rozenfeld, J, Huang, D, Kang, D, Lip, V, Fang, H, Shao, H, Liu, X, Yu, F, Yuan, H, Kenna, M, Miller, DT, Shen, Y, Yang, W, Zelikovic, I, Platt, OS, Han, D, Alper, SL & Wu, BL 2010, '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)', Physiological Genomics, vol. 40, no. 3, pp. 216. https://doi.org/10.1152/physiolgenomics.zh7-3421-corr.2010

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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)

ASJC Scopus subject areas

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