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A missense mutation in DCDC2 causes human recessive deafness DFNB66, likely by interfering with sensory hair cell and supporting cell cilia length regulation.
- Source :
- Human Molecular Genetics; May2015, Vol. 24 Issue 9, p2482-2491, 10p
- Publication Year :
- 2015
Details
- Language :
- English
- ISSN :
- 09646906
- Volume :
- 24
- Issue :
- 9
- Database :
- Complementary Index
- Journal :
- Human Molecular Genetics
- Publication Type :
- Academic Journal
- Accession number :
- 109546333
- Full Text :
- https://doi.org/10.1093/hmg/ddv009