Links
[1] http://omim.org/entry/617110
[2] https://disorders.eyes.arizona.edu/references/bi-allelic-truncating-mutations-cep78-encoding-centrosomal-protein-78-cause-cone-rod
[3] https://disorders.eyes.arizona.edu/references/mutations-cep78-cause-cone-rod-dystrophy-and-hearing-loss-associated-primary-cilia
[4] https://disorders.eyes.arizona.edu/references/cep78-mutated-distinct-type-usher-syndrome