Screening of SLC26A4, FOXI1, KCNJ10, and GJB2 in bilateral deafness patients with inner ear malformation

Otolaryngology - Head and Neck Surgery (United States)

Volumn 146, Issue 6, 2012, Pages 972-978

  Chen, Kaitian ^a   Wang, Xianren ^a   Sun, Liang ^a   Jiang, Hongyan ^a  

^a SUN YAT SEN UNIVERSITY   (China)

Author keywords

FOXI1; GJB2; inner ear malformation; KCNJ10; nonsyndromic sensorineural hearing loss; SLC26A4

Indexed keywords

CONNEXIN 26; FOXI1 PROTEIN; KCNJ10 PROTEIN; PENDRIN; TRANSCRIPTION FACTOR; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; ARTICLE; CHILD; CHINESE; CLINICAL ARTICLE; CROSS-SECTIONAL STUDY; DNA POLYMORPHISM; DNA SEQUENCE; DYSPLASIA; FEMALE; GENE MUTATION; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC SCREENING; GENOTYPE PHENOTYPE CORRELATION; HEARING LOSS; HETEROZYGOTE; HUMAN; INNER EAR MALFORMATION; MALE; PRESCHOOL CHILD; PYROSEQUENCING; SCHOOL CHILD; UNIVERSITY HOSPITAL; VESTIBULE AQUEDUCT;

ADOLESCENT; ADULT; ASIAN CONTINENTAL ANCESTRY GROUP; CHILD; CHILD, PRESCHOOL; CHINA; COHORT STUDIES; CONNEXINS; DEAFNESS; EAR, INNER; FEMALE; FORKHEAD TRANSCRIPTION FACTORS; HEARING LOSS, SENSORINEURAL; HUMANS; MALE; MEMBRANE TRANSPORT PROTEINS; POTASSIUM CHANNELS, INWARDLY RECTIFYING; YOUNG ADULT;

EID: 84864760769     PISSN: 01945998     EISSN: 10976817     Source Type: Journal    
DOI: 10.1177/0194599812439670     Document Type: Article

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