Molecular analysis of hearing loss associated with enlarged vestibular aqueduct in the mainland Chinese: A unique SLC26A4 mutation spectrum

Journal of Human Genetics

Volumn 52, Issue 6, 2007, Pages 492-497

  Hu, Hao ^a   Wu, Lingqian ^a,b,c   Feng, Yong ^a   Pan, Qian ^a   Long, Zhigao ^a   Li, Juan ^a   Dai, Heping ^a   Xia, Kun ^a   Liang, Desheng ^a   Niikawa, Norio ^b,c   Xia, Jiahui ^a  

^a CENTRAL SOUTH UNIVERSITY   (China)

^b NAGASAKI UNIVERSITY GRADUATE SCHOOL OF BIOMEDICAL SCIENCES   (Japan)

^c JAPAN SCIENCE AND TECHNOLOGY AGENCY   (Japan)

Author keywords

Chinese; Enlarged vestibular aqueduct; Molecular analysis; SLC26A4 mutations

Indexed keywords

ADOLESCENT; ADULT; ALLELE; ARTICLE; CHILD; CHINESE; CLINICAL ARTICLE; DATA ANALYSIS; ETHNICITY; FEMALE; GENE; GENE FREQUENCY; GENE MUTATION; GENE SEQUENCE; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC SCREENING; HEARING LOSS; HUMAN; MALE; NUCLEOTIDE SEQUENCE; PENDRED SYNDROME; SLC26A4 GENE; VESTIBULE AQUEDUCT;

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; CHINA; COHORT STUDIES; FEMALE; GOITER; HEARING LOSS, SENSORINEURAL; HUMANS; MALE; MEMBRANE TRANSPORT PROTEINS; MUTATION; VESTIBULAR AQUEDUCT;

EID: 34249741683     PISSN: 14345161     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10038-007-0139-0     Document Type: Article

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