Disease: Deafness- autosomal dominant nonsyndromic sensorineural 53
- A novel MYO6 splice site mutation causes autosomal dominant sensorineural hearing loss type DFNA22 with a favourable outcome after cochlear implantation
- AudioGene: refining the natural history of KCNQ4, GSDME, WFS1, and COCH-associated hearing loss
- Autosomal dominant non-syndromic hearing loss caused by a novel mutation in <em>MYO7A</em>: A case report and review of the literature
- Autosomal dominant non-syndromic hearing loss caused by a novel mutation in MYO7A: A case report and review of the literature
- Benefits of Exome Sequencing in Children with Suspected Isolated Hearing Loss
- Novel mutations confirm that COL11A2 is responsible for autosomal recessive non-syndromic hearing loss DFNB53