Connexin-26 mutations in sporadic non-syndromal sensorineural deafness
- 1 February 1998
- journal article
- research article
- Published by Elsevier in The Lancet
- Vol. 351 (9100) , 415
- https://doi.org/10.1016/s0140-6736(98)24006-2
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- Prelingual Deafness: High Prevalence of a 30delG Mutation in the Connexin 26 GeneHuman Molecular Genetics, 1997
- Connexin26 mutations associated with the most common form of non- syndromic neurosensory autosomal recessive deafness (DFNB1) in MediterraneansHuman Molecular Genetics, 1997
- Connexin 26 mutations in hereditary non-syndromic sensorineural deafnessNature, 1997
- Digenic Retinitis Pigmentosa Due to Mutations at the Unlinked Peripherin/ RDS and ROM1 LociScience, 1994