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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. (2016)

First Author: Davidson AE

Attributed to: The Avon Longitudinal Study of Parents and Children: An international resource for population genomics and lifecourse epidemiology. Core Programme Support 2011-2015 and Core programme support 2014-2019 funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.ajhg.2015.11.018

PubMed Identifier: 26749309

Publication URI: http://europepmc.org/abstract/MED/26749309

Type: Journal Article/Review

Volume: 98

Parent Publication: American journal of human genetics

Issue: 1

ISSN: 0002-9297