Auditory interhemispheric transfer deficits, hearing difficulties, and brain magnetic resonance imaging abnormalities in children with congenital aniridia due to PAX6 mutations

Archives of Pediatrics and Adolescent Medicine

Volumn 161, Issue 5, 2007, Pages 463-469

  Bamiou, Doris Eva ^a,b   Free, Samantha L ^b   Sisodiya, Sanjay M ^b   Chong, Wui K ^d   Musiek, Frank ^f   Williamson, Kathleen A ^g   Van Heyningen, Veronica ^g   Moore, Anthony T ^c   Gadian, David ^a   Luxon, Linda M ^a,e  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

^b UNIVERSITY COLLEGE LONDON   (United Kingdom)

^c MOORFIELDS EYE HOSPITAL   (United Kingdom)

^d GREAT ORMOND STREET HOSPITAL   (United Kingdom)

^e NATIONAL HOSPITAL FOR NEUROLOGY AND NEUROSURGERY   (United Kingdom)

^f UNIVERSITY OF CONNECTICUT   (United States)

^g UNIVERSITY OF EDINBURGH   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

TRANSCRIPTION FACTOR PAX6;

ADOLESCENT; ANIRIDIA; ANTERIOR COMMISSURE; ARTICLE; AUDIOGRAPHY; AUDIOMETRY; AUDITORY NERVOUS SYSTEM; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; CORPUS CALLOSUM; DICHOTIC LISTENING; FEMALE; GENE MUTATION; HEARING IMPAIRMENT; HEARING TEST; HUMAN; INTERHEMISPHERIC TRANSFER; MALE; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; QUESTIONNAIRE; VOLUMETRY;

ADOLESCENT; ADULT; ANIRIDIA; AUDIOMETRY; AUDITORY PERCEPTION; BRAIN DISEASES; CHILD; CHILD, PRESCHOOL; CORPUS CALLOSUM; EYE PROTEINS; FEMALE; HEALTH SURVEYS; HEARING DISORDERS; HEARING TESTS; HOMEODOMAIN PROTEINS; HUMANS; INFANT; INFANT, NEWBORN; MAGNETIC RESONANCE IMAGING; MALE; MIDDLE AGED; MUTATION; PAIRED BOX TRANSCRIPTION FACTORS; POLYMORPHISM, GENETIC; QUESTIONNAIRES; REPRESSOR PROTEINS;

EID: 34248178260     PISSN: 10724710     EISSN: 15383628     Source Type: Journal    
DOI: 10.1001/archpedi.161.5.463     Document Type: Article

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