| Type | Indexed | Publication . Mgi Jnum | J:268488 |
| Publication . Citation | Quinn PM, et al. (2019) Loss of CRB2 in Muller glial cells modifies a CRB1-associated retinitis pigmentosa phenotype into a Leber congenital amaurosis phenotype. Hum Mol Genet 28(1):105-123 |