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Article

Distinct and novel SLC26A4/Pendrin mutations in Chinese and U.S. patients with nonsyndromic hearing loss.

Physiological genomics - 7 Aug 2009

Dai Pu, Stewart Andrew K, Chebib Fouad, Hsu Ann, Rozenfeld Julia, Huang Deliang, Kang Dongyang, Lip Va, Fang Hong, Shao Hong, Liu Xin, Yu Fei, Yuan Huijun, Kenna Margaret, Miller David T, Shen Yiping, Yang Weiyan, Zelikovic Israel, Platt Orah S, Han Dongyi, Alper Seth L, Wu Bai-Lin

Abstract excerpt

Mutations of the human SLC26A4/PDS gene constitute the most common cause of syndromic and nonsyndromic hearing loss. Definition of the SLC26A4 mutation spectrum among different populations with sensorineural hearing loss is important for development of optimal genetic screening services for conge...

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Identifiers

PMID: 19509082
DOI: 10.1152/physiolgenomics.00047.2009

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-19509082-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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