Links
[1] https://disorders.eyes.arizona.edu/disorders/night-blindness-congenital-stationary-csnb1b
[2] http://www.ncbi.nlm.nih.gov/omim/257270
[3] http://ghr.nlm.nih.gov/gene/TRPM1
[4] http://ghr.nlm.nih.gov/gene/GRM6
[5] https://disorders.eyes.arizona.edu/disorders/night-blindness-congenital-stationary-csnb2b
[6] http://www.ncbi.nlm.nih.gov/omim/610427
[7] http://disorders.eyes.arizona.edu/disorders/night-blindness-congenital-stationary
[8] https://disorders.eyes.arizona.edu/references/presentation-trpm1-associated-congenital-stationary-night-blindness-children
[9] https://disorders.eyes.arizona.edu/references/congenital-stationary-night-blindness-hypoplastic-discs-negative-electroretinogram-and
[10] https://disorders.eyes.arizona.edu/references/molecular-basis-human-retinal-and-vitreoretinal-diseases
[11] https://disorders.eyes.arizona.edu/references/recessive-mutations-gene-trpm1-abrogate-bipolar-cell-function-and-cause-complete
[12] https://disorders.eyes.arizona.edu/references/mutations-trpm1-are-common-cause-complete-congenital-stationary-night-blindness