Community Action Needed: Please respond to the NIH RFI
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.
4 Genes / Markers
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)