| |
| | Retina International's Scientific Newsletter - Transducin Mutations |
 | | Dryja, T.P., Hahn, L.B., Reboul, T., and Arnaud, B. Missense mutation in the gene encoding the alpha subunit of rod transducin in the Nougaret form of congenital stationary night blindness. |
 | | Gao, Y.Q., Danciger, M., Akhmedov, N.B., Zhao, D.Y., Heckenlively, J.R., Fishman, G.A., Weleber, R.G., Jacobson, S.G., and Farber, D.B. Exon screening of the genes encoding the beta- and gamma-subunits of cone transducin in patients with inherited retinal disease. |
 | | Magovcevic, I., Weremowicz, S., Morton, C.C., Fong, S.L., Berson, E.L., and Dryja, T.P. Mapping of the human cone transducin alpha-subunit (GNAT2) gene to 1p13 and negative mutation analysis in patients with Stargardt disease. |
| www.retina-international.org /sci-news/gntmut.htm (130 words) |
|