Audiometric analysis of a Belgian family linked to the DFNA10 locus

American Journal of Otology

Volumn 21, Issue 5, 2000, Pages 675-681

  Verstreken, M ^a   Declau, F ^a   Schatteman, I ^a   Van Velzen, D ^a   Verhoeven, K ^a   Van Camp, G ^a   Willems, P J ^a   Kuhweide, E W ^a   Verhaert, E ^a   D'Haese, P ^a   Wuyts, F L ^a   Van de Heyning, P H ^a  

^a UNIVERSITY OF ANTWERP   (Belgium)

Author keywords

Audiometry; DFNA10 locus; Genetic hearing loss; Sensorineural hearing loss

Indexed keywords

ADULT; AGED; ARTICLE; AUDIOMETRY; AUTOSOMAL DOMINANT INHERITANCE; BELGIUM; CHROMOSOME 6; FEMALE; GENE MUTATION; GENETIC DISORDER; GENETIC LINKAGE; HEARING IMPAIRMENT; HUMAN; MAJOR CLINICAL STUDY; MALE; ONSET AGE; PEDIGREE; PERCEPTION DEAFNESS; PHENOTYPE; PRIORITY JOURNAL; TINNITUS; VERTIGO;

ADULT; AGED; AGING; AUDIOMETRY, PURE-TONE; AUDITORY THRESHOLD; BELGIUM; CROSS-SECTIONAL STUDIES; FEMALE; GENE EXPRESSION; HEARING LOSS, SENSORINEURAL; HUMANS; MALE; MIDDLE AGED; PEDIGREE; RETROSPECTIVE STUDIES; SEVERITY OF ILLNESS INDEX; VESTIBULE;

EID: 0033858735     PISSN: 01929763     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (15)

1. Mouse models for human hearing impairment
2. A gene for autosomal dominant late-onset progressive non-syndromic hearing loss, DFNA 10, maps to chromosome 6
3. Dominant hereditary nerve deafness
4. Dominant midfrequency hearing loss
5. Hereditary nerve deafness
6. A gene for autosomal dominant nonsyndromic hearing loss (DFNA 12) maps to chromosome 11q22-24
7. Mutations in the human alpha-tectorin gene cause autosomal dominant nonsyndromic hearing impairment
8. A new autosomal dominant locus (DFNA 12) is responsible for a nonsyndromic, midfrequency, prelingual and nonprogressive sensorineural hearing loss
9. A novel locus for autosomal dominant nonsyndromic hearing loss, DFNA 13, maps to chromosome 6p
10. Linkage of a gene for dominant non-syndromic deafness to chromosome 19
11. A gene for a dominant form of non-syndromic sensorineural deafness (DFNA 11) maps within the region containing the DFNB2 recessive deafness gene