Back to Search
Start Over
Mutations in SDCCAG8/NPHP10 Cause Bardet-Biedl Syndrome and Are Associated with Penetrant Renal Disease and Absent Polydactyly.
- Source :
- Molecular Syndromology; 2010, Vol. 1 Issue 6, p273-281, 9p
- Publication Year :
- 2010
Details
- Language :
- English
- ISSN :
- 16618769
- Volume :
- 1
- Issue :
- 6
- Database :
- Complementary Index
- Journal :
- Molecular Syndromology
- Publication Type :
- Academic Journal
- Accession number :
- 67450565
- Full Text :
- https://doi.org/10.1159/000331268