Links
[1] http://ghr.nlm.nih.gov/gene/MYO7A
[2] http://www.ncbi.nlm.nih.gov/omim/276900
[3] http://ghr.nlm.nih.gov/gene/USH1C
[4] http://www.ncbi.nlm.nih.gov/omim/276904
[5] http://ghr.nlm.nih.gov/gene/CDH23
[6] http://www.ncbi.nlm.nih.gov/omim/601067
[7] http://ghr.nlm.nih.gov/gene/PCDH15
[8] http://www.ncbi.nlm.nih.gov/omim/602083
[9] http://ghr.nlm.nih.gov/gene/USH1G
[10] http://www.ncbi.nlm.nih.gov/omim/606943
[11] http://www.ncbi.nlm.nih.gov/omim/602097
[12] http://www.ncbi.nlm.nih.gov/omim/612632
[13] http://ghr.nlm.nih.gov/gene/ABCC8
[14] http://ghr.nlm.nih.gov/gene/KCNJ11
[15] http://omim.org/entry/606528
[16] https://disorders.eyes.arizona.edu/disorders/usher-syndrome-type-ii
[17] http://www.ncbi.nlm.nih.gov/omim/276901
[18] https://disorders.eyes.arizona.edu/disorders/usher-syndrome-type-iii
[19] http://www.ncbi.nlm.nih.gov/omim/276902
[20] http://ghr.nlm.nih.gov/gene/CLRN1
[21] https://disorders.eyes.arizona.edu/references/targeted-exon-sequencing-usher-syndrome-type-i
[22] https://disorders.eyes.arizona.edu/references/clinical-aspects-usher-syndrome-and-ush2a-gene-cohort-433-patients
[23] https://disorders.eyes.arizona.edu/references/heterogeneity-phenotype-usher-congenital-hyperinsulinism-syndrome-hearing-loss-retinitis
[24] https://disorders.eyes.arizona.edu/references/ush1k-novel-locus-type-i-usher-syndrome-maps-chromosome-10p1121-q21
[25] https://disorders.eyes.arizona.edu/references/molecular-genetics-usher-syndrome
[26] https://disorders.eyes.arizona.edu/references/clinical-diagnosis-usher-syndromes-usher-syndrome-consortium