Links
[1] http://www.ncbi.nlm.nih.gov/omim/304020
[2] http://ghr.nlm.nih.gov/gene/RPGR
[3] http://www.ncbi.nlm.nih.gov/omim/300455
[4] http://www.ncbi.nlm.nih.gov/omim/300029
[5] http://omim.org/entry/244400
[6] http://www.ncbi.nlm.nih.gov/omim/300085
[7] http://www.ncbi.nlm.nih.gov/omim/300476
[8] http://ghr.nlm.nih.gov/gene/CACNA1F
[9] https://disorders.eyes.arizona.edu/disorders/night-blindness-congenital-stationary-csnb2a
[10] http://www.ncbi.nlm.nih.gov/omim/300071
[11] https://disorders.eyes.arizona.edu/disorders/aland-island-eye-disease
[12] http://omim.org/entry/300600
[13] https://disorders.eyes.arizona.edu/references/x-linked-cone-rod-dystrophy-cordx3-caused-mutation-cacna1f-gene
[14] https://disorders.eyes.arizona.edu/references/mutations-rpgr-gene-cause-x-linked-cone-dystrophy
[15] https://disorders.eyes.arizona.edu/references/localization-novel-x-linked-progressive-cone-dystrophy-gene-xq27-evidence-genetic
[16] https://disorders.eyes.arizona.edu/references/clinical-diversity-and-chromosomal-localization-x-linked-cone-dystrophy-cod1