Back to Search
Start Over
Clinical Studies of Families With Hearing Loss Attributable to Mutations in the Connexin 26 Gene (GJB2/DFNB1).
- Source :
-
Pediatrics . Mar99, Vol. 103 Issue 3, p546. 5p. - Publication Year :
- 1999
-
Abstract
- Presents information on a study regarding genetic hearing loss caused by mutations in the connexin 26 (Cx26) gene. Summary of the clinical trials; Characteristics of the Cx26 patients; Assessment on their hearing impairment.
- Subjects :
- *GENETICS of deafness
*CONNEXINS
*GENETIC mutation
Subjects
Details
- Language :
- English
- ISSN :
- 00314005
- Volume :
- 103
- Issue :
- 3
- Database :
- Academic Search Index
- Journal :
- Pediatrics
- Publication Type :
- Academic Journal
- Accession number :
- 1681947
- Full Text :
- https://doi.org/10.1542/peds.103.3.546