Ccdc66 null mutation causes retinal degeneration and dysfunctionWanda M. Gerding(Ruhr University Bochum), Elisabeth Petrasch‐Parwez(University Hospitals of the Ruhr-University of Bochum)Human Molecular GeneticsJune 16, 201110.1093/hmg/ddr282Cited by 47SaveCiteExport RISWatch citationsRelated PapersSignal transducer and activator of transcription 3-mediated regulation of miR-199a-5p links cardiomyocyte and endothelial cell function in the heart: a key role for ubiquitin-conjugating enzymes|European Heart Journal|2010|134