The DFNA 10 phenotype

Annals of Otology, Rhinology and Laryngology

Volumn 110, Issue 9, 2001, Pages 861-866

  De Leenheer, Els M R ^a   Huygen, Patrick L M ^a   Smith, Richard J H ^a   Wayne, Sigrid ^a   Cremers, Cor W R J ^a  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

Autosomal dominant nonsyndromic hearing loss; DFNA10; Speech discrimination

Indexed keywords

ADOLESCENT; ADULT; AGED; ARTICLE; AUDIOMETRY; AUDITORY THRESHOLD; CROSS-SECTIONAL STUDY; DISEASE COURSE; DOMINANT GENE; GENETICS; HEARING; HEARING IMPAIRMENT; HUMAN; MIDDLE AGED; PATHOPHYSIOLOGY; PEDIGREE; PHENOTYPE; SPEECH PERCEPTION; AUTOSOMAL DOMINANT DISORDER; CHROMOSOME 6Q; CLINICAL ARTICLE; DFNA10 GENE; GENE; GENE LOCUS; HEARING LOSS; PERCEPTION DEAFNESS; PRESBYACUSIS; PRIORITY JOURNAL; REGRESSION ANALYSIS; SPEECH DISCRIMINATION;

ADOLESCENT; ADULT; AGED; AGED, 80 AND OVER; AUDIOMETRY; AUDITORY THRESHOLD; CROSS-SECTIONAL STUDIES; DEAFNESS; DISEASE PROGRESSION; GENES, DOMINANT; HEARING; HUMANS; MIDDLE AGED; PEDIGREE; PHENOTYPE; SPEECH PERCEPTION;

EID: 0034741745     PISSN: 00034894     EISSN: None     Source Type: Journal    
DOI: 10.1177/000348940111000910     Document Type: Article

References (5)

1. A gene for autosomal dominant late-onset progressive non-syndromic hearing loss, DFNA10, maps to chromosome 6