Autosomal-Dominant Corneal Endothelial Dystrophies CHED1 and PPCD1 Are Allelic Disorders Caused by Non-coding Mutations in the Promoter of OVOL2-Reference-Cited by-同舟云学术

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

Published:2016-01 Issue:1 Volume:98 Page:75-89
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

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.

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference49 articles.

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