Autosomal-Dominant Corneal Endothelial Dystrophies CHED1 and PPCD1 Are Allelic Disorders Caused by Non-coding Mutations in the Promoter of OVOL2
Titel:
Autosomal-Dominant Corneal Endothelial Dystrophies CHED1 and PPCD1 Are Allelic Disorders Caused by Non-coding Mutations in the Promoter of OVOL2
Auteur:
Davidson, Alice E. Liskova, Petra Evans, Cerys J. Dudakova, Lubica Nosková, Lenka Pontikos, Nikolas Hartmannová, Hana Hodaňová, Kateřina Stránecký, Viktor Kozmík, Zbyněk Levis, Hannah J. Idigo, Nwamaka Sasai, Noriaki Maher, Geoffrey J. Bellingham, James Veli, Neyme Ebenezer, Neil D. Cheetham, Michael E. Daniels, Julie T. Thaung, Caroline M.H. Jirsova, Katerina Plagnol, Vincent Filipec, Martin Kmoch, Stanislav Tuft, Stephen J. Hardcastle, Alison J.