Links
[1] http://omim.org/entry/204000
[2] http://ghr.nlm.nih.gov/gene/GUCY2D
[3] http://omim.org/entry/204100
[4] http://ghr.nlm.nih.gov/gene/RPE65
[5] http://omim.org/entry/604232
[6] http://ghr.nlm.nih.gov/gene/SPATA7
[7] http://omim.org/entry/604393
[8] http://ghr.nlm.nih.gov/gene/AIPL1
[9] http://omim.org/entry/604537
[10] http://ghr.nlm.nih.gov/gene/LCA5
[11] http://omim.org/entry/613826
[12] http://ghr.nlm.nih.gov/gene/RPGRIP1
[13] http://omim.org/entry/613829
[14] http://ghr.nlm.nih.gov/gene/CRX
[15] http://omim.org/entry/613835
[16] http://ghr.nlm.nih.gov/gene/CRB1
[17] http://omim.org/entry/608553
[18] http://ghr.nlm.nih.gov/gene/NMNAT1
[19] http://omim.org/entry/611755
[20] http://ghr.nlm.nih.gov/gene/CEP290
[21] http://omim.org/entry/613837
[22] http://ghr.nlm.nih.gov/gene/IMPDH1
[23] http://omim.org/entry/610612
[24] http://ghr.nlm.nih.gov/gene/RD3
[25] http://omim.org/entry/612712
[26] http://ghr.nlm.nih.gov/gene/RDH12
[27] http://omim.org/entry/613341
[28] http://ghr.nlm.nih.gov/gene/LRAT
[29] http://omim.org/entry/613843
[30] http://ghr.nlm.nih.gov/gene/TULP1
[31] http://omim.org/entry/614186
[32] http://ghr.nlm.nih.gov/gene/KCNJ13
[33] http://www.omim.org/entry/615360
[34] http://ghr.nlm.nih.gov/gene/GDF6
[35] http://omim.org/entry/608133
[36] http://omim.org/entry/179605
[37] http://omim.org/entry/613794
[38] https://disorders.eyes.arizona.edu/disorders/leber-congenital-amaurosis-early-onset-deafness
[39] https://disorders.eyes.arizona.edu/references/leber-congenital-amaurosisearly-onset-severe-retinal-dystrophy-clinical-features
[40] https://disorders.eyes.arizona.edu/references/omics-ophthalmology-advances-genomics-and-precision
[41] https://disorders.eyes.arizona.edu/references/autosomal-dominant-leber-congenital-amaurosis-caused-heterozygous-crx-mutation-father-and
[42] https://disorders.eyes.arizona.edu/references/mutations-nmnat1-cause-leber-congenital-amaurosis-and-identify-new-disease
[43] https://disorders.eyes.arizona.edu/references/dominant-mutation-rpe65-identified-whole-exome-sequencing-causes-retinitis-pigmentosa-cho
[44] https://disorders.eyes.arizona.edu/references/treatment-leber-congenital-amaurosis-due-rpe65-mutations-ocular-subretinal-injection
[45] https://disorders.eyes.arizona.edu/references/effect-gene-therapy-visual-function-lebers-congenital-amaurosis
[46] https://disorders.eyes.arizona.edu/references/genotyping-microarray-disease-chip-leber-congenital-amaurosis-detection-modifier-alleles
[47] https://disorders.eyes.arizona.edu/references/leber-congenital-amaurosis
[48] https://disorders.eyes.arizona.edu/references/clinical-phenotypes-carriers-leber-congenital-amaurosis-mutations
[49] https://disorders.eyes.arizona.edu/references/recessive-mutations-kcnj13-encoding-inwardly-rectifying-potassium-channel-subunit-cause