SLC26A4 c.919-2A>G varies among Chinese ethnic groups as a cause of hearing loss

Genetics in Medicine

Volumn 10, Issue 8, 2008, Pages 586-592

  Dai, Pu ^a   Li, Qi ^a   Huang, Deliang ^a   Yuan, Yongyi ^a   Kang, Dongyang ^a   Miller, David T ^b   Shao, Hong ^b   Zhu, Qingwen ^a   He, Jia ^c   Yu, Fei ^a   Liu, Xin ^a   Han, Bing ^a   Yuan, Huijun ^a   Platt, Orah S ^b   Han, Dongyi ^a   Wu, Bai Lin ^b  

^a CHINESE PLA GENERAL HOSPITAL   (China)

^b BOSTON CHILDREN S HOSPITAL   (United States)

^c SECOND MILITARY MEDICAL UNIVERSITY   (China)

Author keywords

c.919 2A>G (IVS7 2A>G); Chinese; Deafness; DNA diagnostics; Genetic epidemiology; Hearing loss; SLC26A4; SNHL

Indexed keywords

PENDRIN;

ADOLESCENT; ADULT; ARTICLE; CHILD; CHINESE; CONTROLLED STUDY; ETHNIC GROUP; FEMALE; GENE FREQUENCY; GENE MUTATION; GENOTYPE; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; MAJOR CLINICAL STUDY; MALE; PERCEPTION DEAFNESS; PREVALENCE; RESTRICTION FRAGMENT LENGTH POLYMORPHISM;

ADOLESCENT; ASIAN CONTINENTAL ANCESTRY GROUP; CHILD; CHILD, PRESCHOOL; CHINA; FEMALE; GENE FREQUENCY; GENETIC VARIATION; GEOGRAPHY; HEARING LOSS, SENSORINEURAL; HUMANS; MALE; MEMBRANE TRANSPORT PROTEINS; MUTATION; PREVALENCE; YOUNG ADULT;

EID: 55849085776     PISSN: 10983600     EISSN: None     Source Type: Journal    
DOI: 10.1097/GIM.0b013e31817d2ef1     Document Type: Article

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