Case report: a novel KERA mutation associated with cornea plana and its predicted effect on protein function

Corneal Endothelial Findings in a Czech Patient with Compound Heterozygous Mutations inKERA

(2013) Lubica Dudakova et al.   OPHTHALMIC GENETICS

An integrated map of genetic variation from 1,092 human genomes

(2012)   NATURE

Evolution and Functional Impact of Rare Coding Variation from Deep Sequencing of Human Exomes

(2012) J. A. Tennessen et al.   SCIENCE

LRRfinder: A web application for the identification of leucine-rich repeats and an integrative Toll-like receptor database

(2010) V. Offord et al.   DEVELOPMENTAL AND COMPARATIVE IMMUNOLOGY

The molecular basis of corneal transparency

(2010) John R. Hassell et al.   EXPERIMENTAL EYE RESEARCH

A method and server for predicting damaging missense mutations

(2010) Ivan A Adzhubei et al.   NATURE METHODS

Corneal Decompensation in Recessive Cornea Plana

(2009) Arif O. Khan et al.   OPHTHALMIC GENETICS

The leucine-rich repeat structure

(2008) J. Bella et al.   CELLULAR AND MOLECULAR LIFE SCIENCES