Genetics of the corneal endothelial dystrophies: an evidence-based review

Association of TCF4 and CLU polymorphisms with Fuchs’ endothelial dystrophy and implication of CLU and TGFBI proteins in the disease process

(2012) Abraham Kuot et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

A Common Trinucleotide Repeat Expansion within the Transcription Factor 4 (TCF4, E2-2) Gene Predicts Fuchs Corneal Dystrophy

(2012) Eric D. Wieben et al.   PLoS One

Differing Roles for TCF4 and COL8A2 in Central Corneal Thickness and Fuchs Endothelial Corneal Dystrophy

(2012) Robert P. Igo et al.   PLoS One

Replication of TCF4 through Association and Linkage Studies in Late-Onset Fuchs Endothelial Corneal Dystrophy

(2011) Yi-Ju Li et al.   PLoS One

Missense Mutations in TCF8 Cause Late-Onset Fuchs Corneal Dystrophy and Interact with FCD4 on Chromosome 9p

(2010) S. Amer Riazuddin et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Missense mutations in the sodium borate cotransporter SLC4A11 cause late-onset Fuchs corneal dystrophya

(2010) S. Amer Riazuddin et al.   HUMAN MUTATION

E2-2 Protein and Fuchs's Corneal Dystrophy

(2010) Keith H. Baratz et al.   NEW ENGLAND JOURNAL OF MEDICINE

The PPCD1 Mouse: Characterization of a Mouse Model for Posterior Polymorphous Corneal Dystrophy and Identification of a Candidate Gene

(2010) Anna L. Shen et al.   PLoS One

DYSTROPHIA CORNEAE PARENCHYMATOSA CONGENITA A CLINICAL, MORPHOLOGICAL AND HISTOCHEMICAL EXAMINATION

(2009) Magnus Odland   ACTA OPHTHALMOLOGICA

Clinical phenotype of posterior polymorphous corneal dystrophy in a family with a novel ZEB1 mutation

(2009) Dan Q. Nguyen et al.   ACTA OPHTHALMOLOGICA

Identification of Mutations in the SLC4A11 Gene in Patients With Recessive Congenital Hereditary Endothelial Dystrophy

(2008) Boomiraj Hemadevi   ARCHIVES OF OPHTHALMOLOGY

The role of the ZEB family of transcription factors in development and disease

(2008) C. Vandewalle et al.   CELLULAR AND MOLECULAR LIFE SCIENCES

Zeb1 links epithelial-mesenchymal transition and cellular senescence

(2008) Y. Liu et al.   DEVELOPMENT

Q455V mutation in COL8A2 is associated with Fuchs' corneal dystrophy in Korean patients

(2008) J-W Mok et al.   EYE

Mutation in theSLC4A11Gene Associated with Autosomal Recessive Congenital Hereditary Endothelial Dystrophy in a Large Saudi Family

(2008) Shaival S. Shah et al.   OPHTHALMIC GENETICS