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.
CRISPR List (2 Records)
Target Reagent
rcbtb1 CRISPR1-rcbtb1
CRISPR2-rcbtb1
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