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

Volumn 40, Issue 3, 2010, Pages 216-

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

^a NONE

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ERRATUM; ERROR; PRIORITY JOURNAL;

EID: 76549094239     PISSN: 10948341     EISSN: 15312267     Source Type: Journal    
DOI: 10.1152/physiolgenomics.zh7-3421-corr.2010     Document Type: Erratum

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