Mutations in the IMPG2, encodinginterphotoreceptor matrix proteoglycan 2, cause autosomal recessive retinitis pigmentosa.

Bandah-Rozenfeld, D., Collin, R.W.J., Banin, E., L. van den Born, I., Coene, K.L.M., Siemiatkowska, A.M., Zelinger, L., Khan, M.I., Lefeber, D.J., Erdinest, I., Testa, F., Simonelli, F., Voesenek. K., Blokland, E.A.W., Strom, T.M., Klaver, C.C.W., Qamar, R., Banfi, S., Cremers, F.P.M., Sharon, D., den Hollander, A.I.  

American Journal of Human Genetics, 87:199-208  (2010).