Links
[1] http://ghr.nlm.nih.gov/gene/CLRN1
[2] http://omim.org/entry/614504
[3] http://ghr.nlm.nih.gov/gene/HARS
[4] https://disorders.eyes.arizona.edu/disorders/retinitis-pigmentosa-hearing-loss-ataxia-cataract-and-polyneuropathy
[5] http://omim.org/entry/612674
[6] https://disorders.eyes.arizona.edu/disorders/usher-syndrome-type-i
[7] http://www.ncbi.nlm.nih.gov/omim/276900
[8] https://disorders.eyes.arizona.edu/disorders/usher-syndrome-type-ii
[9] http://www.ncbi.nlm.nih.gov/omim/276901
[10] https://disorders.eyes.arizona.edu/references/targeted-next-generation-sequencing-identifies-homozygous-nonsense-mutation-abhd12-gene
[11] https://disorders.eyes.arizona.edu/references/usher-syndrome-iiia-gene-clarin-1-essential-hair-cell-function-and-associated-neural
[12] https://disorders.eyes.arizona.edu/references/mutation-screening-ush3-gene-clarin-1-spanish-patients-usher-syndrome-low-prevalence-and
[13] https://disorders.eyes.arizona.edu/references/ophthalmological-course-usher-syndrome-type-iii