Work

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

Year: 2009

Type: article

Study design: Observational Study

Source: Physiological Genomics

DOI: 10.1152/physiolgenomics.00047.2009

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

Institutions: Chinese PLA General Hospital, Chinese People's Liberation Army, Beth Israel Deaconess Medical Center, Harvard University, Technion – Israel Institute of Technology, Rambam Health Care Campus, Boston Children's Hospital, Fudan University

Language: English

Topic: Hearing, Cochlea, Tinnitus, Genetics

Subfield: Sensory Systems

Field: Neuroscience

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W2102180389

FWCI: 2.668

Cites: 40

Cited by: 64

Related to: 10