Links
[1] http://ghr.nlm.nih.gov/gene/CRB1
[2] https://disorders.eyes.arizona.edu/disorders/nanophthalmos-retinitis-pigmentosa
[3] https://disorders.eyes.arizona.edu/disorders/pigmented-paravenous-chorioretinal-atrophy
[4] http://omim.org/entry/172870
[5] http://omim.org/entry/600105
[6] https://disorders.eyes.arizona.edu/disorders/leber-congenital-amaurosis
[7] http://omim.org/entry/613835
[8] https://disorders.eyes.arizona.edu/references/whole-exome-sequencing-identifies-crb1-defect-unusual-maculopathy-phenotype
[9] https://disorders.eyes.arizona.edu/references/natural-course-ocular-function-pigmented-paravenous-retinochoroidal-atrophy
[10] https://disorders.eyes.arizona.edu/references/pigmented-paravenous-chorioretinal-atrophy-associated-mutation-within-crumbs-homolog
[11] https://disorders.eyes.arizona.edu/references/hereditary-pigmented-paravenous-chorioretinal-atrophy
[12] https://disorders.eyes.arizona.edu/references/progressive-nature-pigmented-paravenous-retinochoroidal-atrophy