Links
[1] http://ghr.nlm.nih.gov/gene/EPHA2
[2] https://disorders.eyes.arizona.edu/disorders/cataracts-congenital-volkmann-type
[3] http://disorders.eyes.arizona.edu/omim/115665
[4] https://disorders.eyes.arizona.edu/disorders/cataracts-congenital-cerulean
[5] http://www.ncbi.nlm.nih.gov/omim/115660
[6] http://www.ncbi.nlm.nih.gov/omim/601547
[7] http://www.ncbi.nlm.nih.gov/omim/608983
[8] http://www.ncbi.nlm.nih.gov/omim/610202
[9] https://disorders.eyes.arizona.edu/disorders/cataracts-coppock
[10] http://www.ncbi.nlm.nih.gov/omim/604307
[11] https://disorders.eyes.arizona.edu/disorders/cataracts-lamellar
[12] http://www.ncbi.nlm.nih.gov/omim/116800
[13] https://disorders.eyes.arizona.edu/references/identification-novel-c-terminal-extension-mutation-epha2-family-affected-congenital-catar
[14] https://disorders.eyes.arizona.edu/references/mutations-epha2-receptor-tyrosine-kinase-gene-cause-autosomal-dominant-congenital
[15] https://disorders.eyes.arizona.edu/references/epha2-gene-associated-cataracts-linked-chromosome-1p