OBO ID: DOID:0050795

Citations

(4 total)

Term: cone dystrophy

Kohl, S., Llavona, P., Sauer, A., Reuter, P., Weisschuh, N., Kempf, M., Dehmelt, F.A., Arrenberg, A.B., Sliesoraityte, I., Zrenner, E., van Schooneveld, M.J., Rudolph, G., Kühlewein, L., Wissinger, B. (2021) A duplication on chromosome 16q12 affecting the IRXB gene cluster is associated with autosomal dominant cone dystrophy with early tritanopic color vision defect. Human molecular genetics. 30(13):1218-1229

Clark, E.M., Nonarath, H.J.T., Bostrom, J.R., Link, B.A. (2019) Establishment and validation of an endoplasmic reticulum stress reporter to monitor zebrafish ATF6 activity in development and disease. Disease models & mechanisms. 13(1):

Schlegel, D.K., Glasauer, S.M.K., Mateos, J.M., Barmettler, G., Ziegler, U., Neuhauss, S.C.F. (2019) A New Zebrafish Model for CACNA2D4-Dysfunction. Investigative ophthalmology & visual science. 60:5124-5135

Link, B.A., Collery, R.F. (2015) Zebrafish Models of Retinal Disease. Annual review of vision science. 1:125-153