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Allele Publication :

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

1 Publication