The influence of mutations in the SLC26A4 gene on the temporal bone in a population with enlarged vestibular aqueduct

Archives of Otolaryngology - Head and Neck Surgery

Volumn 133, Issue 2, 2007, Pages 162-168

  Madden, Colm ^a   Halsted, Mark ^b,c   Meinzen Derr, Jareen ^b   Bardo, Dianna ^d   Boston, Mark ^b   Arjmand, Ellis ^b,c   Nishimura, Carla ^e   Yang, Tao ^e   Benton, Corning ^b,c   Das, Vijay ^a   Smith, Richard ^e   Choo, Daniel ^b,c   Greinwald, John ^b,c  

^a MANCHESTER ROYAL INFIRMARY   (United Kingdom)

^b CINCINNATI CHILDREN'S HOSPITAL MEDICAL CENTER   (United States)

^c UNIVERSITY OF CINCINNATI COLLEGE OF MEDICINE   (United States)

^d UNIVERSITY OF CHICAGO   (United States)

^e UNIVERSITY OF IOWA HEALTH CARE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

PENDRIN; SOLUTE CARRIER FAMILY 26 MEMBER 4; UNCLASSIFIED DRUG;

ADOLESCENT; ALLELE; ARTICLE; AUDIOMETRY; BONE RADIOGRAPHY; CHILD; CONTROLLED STUDY; DATA BASE; FEMALE; GENE; GENE MUTATION; GENETIC SCREENING; GENOTYPE PHENOTYPE CORRELATION; HEARING IMPAIRMENT; HEARING LOSS; HUMAN; INFANT; MAJOR CLINICAL STUDY; MALE; OUTCOME ASSESSMENT; PENDRED SYNDROME; PURE TONE AUDIOMETRY; RADIODIAGNOSIS; RETROSPECTIVE STUDY; SOUND INTENSITY; STATISTICAL SIGNIFICANCE; TEMPORAL BONE; TERTIARY HEALTH CARE; VESTIBULE; VESTIBULE AQUEDUCT;

ADOLESCENT; ADULT; AUDIOMETRY, PURE-TONE; CHILD; CHILD, PRESCHOOL; FEMALE; GENOTYPE; HEARING LOSS, SENSORINEURAL; HUMANS; INFANT; MALE; MEMBRANE TRANSPORT PROTEINS; MUTATION; PHENOTYPE; RETROSPECTIVE STUDIES; TEMPORAL BONE; VESTIBULAR AQUEDUCT;

EID: 33847167581     PISSN: 08864470     EISSN: 08864470     Source Type: Journal    
DOI: 10.1001/archotol.133.2.162     Document Type: Article

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