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Autosomal-Dominant Corneal Endothelial Dystrophies CHED1 and PPCD1 Are Allelic Disorders Caused by Non-coding Mutations in the Promoter of OVOL2

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Description scientific article
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author: Kateřina Jirsová  Nikolas Pontikos  Alison Hardcastle  Hannah J. Levis  Kateřina Hodaňová  Petra Lišková  Geoffrey Maher  Michael E. Cheetham  Noriaki Sasai  Viktor Stránecký  Lenka Noskova  Hana Hartmannová  Ľubica Ďuďáková  Caroline Thaung 

Publication date December 31, 2015
Language English
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