## Abstract Nonsyndromic autosomal dominant sensorineural hearing loss (SNHL) at the DFNA10 locus was described in two families in 2001. Causative mutations that affect the EyaHR domain of the βEyes absent 4β (EYA4) protein were identified. We report on the clinical and genetic analyses of an Austr
A novel splice site mutation in the RDX gene causes DFNB24 hearing loss in an Iranian family
β Scribed by A. Eliot Shearer; Michael S. Hildebrand; Catherine J. Bromhead; Kimia Kahrizi; Jennifer A. Webster; Batool Azadeh; William J. Kimberling; Ali Anousheh; Arash Nazeri; Dietrich Stephan; Hossein Najmabadi; Richard J.H. Smith; Melanie Bahlo
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 192 KB
- Volume
- 149A
- Category
- Article
- ISSN
- 1552-4825
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