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Usher syndromes due to MYO7A, PCDH15, USH2A or GPR98 mutations share retinal disease mechanism.
- Source :
- Human Molecular Genetics; Aug2008, Vol. 17 Issue 15, p2405-2415, 11p
- Publication Year :
- 2008
Details
- Language :
- English
- ISSN :
- 09646906
- Volume :
- 17
- Issue :
- 15
- Database :
- Complementary Index
- Journal :
- Human Molecular Genetics
- Publication Type :
- Academic Journal
- Accession number :
- 44556209
- Full Text :
- https://doi.org/10.1093/hmg/ddn140