Connexin 26 gene linked to a dominant deafness
- 1 May 1998
- journal article
- research article
- Published by Springer Nature in Nature
- Vol. 393 (6683) , 319-320
- https://doi.org/10.1038/30639
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
- Connexin mutations and hearing lossNature, 1998
- Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA geneNature Genetics, 1997
- The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA geneNature Genetics, 1997
- Mutations in the myosin VIIA gene cause non-syndromic recessive deafnessNature Genetics, 1997
- Connexin 26 mutations in hereditary non-syndromic sensorineural deafnessNature, 1997
- The Role of the Gap Junction Protein Connexin32 in the Myelin SheathPublished by Springer Nature ,1997
- Genes responsible for human hereditary deafness: symphony of a thousandNature Genetics, 1996