Wu et al., 2016 - Haploinsufficiency of RCBTB1 is Associated with Coats Disease and Familial Exudative Vitreoretinopathy. Human molecular genetics   25(8):1637-47 Full text @ Hum. Mol. Genet.
Morpholino List (3 Records)
Target Reagent
ndp MO1-ndp
rcbtb1 MO1-rcbtb1
MO2-rcbtb1