Phenotypic analyses and mutation screening of the SLC26A4 and FOXI1 genes in 101 Taiwanese families with bilateral nonsyndromic enlarged vestibular aqueduct (DFNB4) or pendred syndrome

Audiology and Neurotology

Volumn 15, Issue 1, 2010, Pages 57-66

  Wu, Chen Chi ^a,b   Lu, Ying Chang ^a,c   Chen, Pei Jer ^b   Yeh, Po Lin ^a   Su, Yi Nin ^b   Hwu, Wuh Liang ^b   Hsu, Chuan Jen ^a  

^a NATIONAL TAIWAN UNIVERSITY HOSPITAL   (Taiwan)

^b NATIONAL TAIWAN UNIVERSITY   (Taiwan)

^c NATIONAL TAIWAN UNIVERSITY   (Taiwan)

Author keywords

Enlarged vestibular aqueduct; FOXI1; Haplotype; Pendred syndrome; SLC26A4

Indexed keywords

DNA FRAGMENT; TRANSCRIPTION FACTOR;

ACCURACY; ADOLESCENT; ADULT; ALLELE; ARTICLE; AUDIOLOGY; CHILD; EXON; EXPLORATORY BEHAVIOR; FAMILY; GENE CONTROL; GENE MUTATION; GENE SEQUENCE; GENETIC CODE; GENETIC COUNSELING; GENETIC SCREENING; GENETIC TRANSCRIPTION; GENETIC VARIABILITY; GENOMIC FRAGMENT; GENOTYPE; GOITER; HAPLOTYPE; HETEROZYGOTE; HUMAN; INFANT; INTRON; MAJOR CLINICAL STUDY; MICROBIAL DIVERSITY; NONSYNDROMIC ENLARGED VESTIBULAR AQUEDUCT; PATHOLOGY; PENDRED SYNDROME; PHENOTYPE; POLYMERASE CHAIN REACTION; PRESCHOOL CHILD; PRIORITY JOURNAL; PROMOTER REGION; QUANTITATIVE ANALYSIS; RADIOLOGY; SCHOOL CHILD; TAIWAN; VESTIBULAR DISORDER; VESTIBULE AQUEDUCT;

EID: 84984593150     PISSN: 14203030     EISSN: 14219700     Source Type: Journal    
DOI: 10.1159/000231567     Document Type: Article

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