Back to Search
Start Over
Mutations in IFT172 cause isolated retinal degeneration and Bardet–Biedl syndrome.
- Source :
- Human Molecular Genetics; Jan2015, Vol. 24 Issue 1, p230-242, 13p, 3 Color Photographs, 1 Diagram, 2 Charts, 1 Graph
- Publication Year :
- 2015
Details
- Language :
- English
- ISSN :
- 09646906
- Volume :
- 24
- Issue :
- 1
- Database :
- Complementary Index
- Journal :
- Human Molecular Genetics
- Publication Type :
- Academic Journal
- Accession number :
- 119562441
- Full Text :
- https://doi.org/10.1093/hmg/ddu441