Ebermann et al., 2010
- PDZD7 is a modifier of retinal disease and a contributor to digenic Usher syndrome.
J. Clin. Invest.
120(6):1812-1823
Full text @ J. Clin. Invest.
| Marker Type | Symbol | Name |
|---|---|---|
| Gene | adgrv1 | adhesion G protein-coupled receptor V1 |
| Gene | pdzd7a | PDZ domain containing 7a |
| Gene | pdzd7b | PDZ domain containing 7b |
| Gene | ush2a | Usher syndrome 2A (autosomal recessive, mild) |