Christina Zeitz
Institute of Medical Genetics
Division of Medical Molecular Genetics and Gene Diagnostics
University of Zurich
Zurich
Switzerland
Name/email consistency: high
- Night blindness-associated mutations in the ligand-binding, cysteine-rich, and intracellular domains of the metabotropic glutamate receptor 6 abolish protein trafficking. Zeitz, C., Forster, U., Neidhardt, J., Feil, S., Kälin, S., Leifert, D., Flor, P.J., Berger, W. Hum. Mutat. (2007)
- Mutations in CABP4, the gene encoding the Ca2+-binding protein 4, cause autosomal recessive night blindness. Zeitz, C., Kloeckener-Gruissem, B., Forster, U., Kohl, S., Magyar, I., Wissinger, B., Mátyás, G., Borruat, F.X., Schorderet, D.F., Zrenner, E., Munier, F.L., Berger, W. Am. J. Hum. Genet. (2006)
- Novel mutations in CACNA1F and NYX in Dutch families with X-linked congenital stationary night blindness. Zeitz, C., Minotti, R., Feil, S., Mátyás, G., Cremers, F.P., Hoyng, C.B., Berger, W. Mol. Vis. (2005)
- Mutations in GRM6 cause autosomal recessive congenital stationary night blindness with a distinctive scotopic 15-Hz flicker electroretinogram. Zeitz, C., van Genderen, M., Neidhardt, J., Luhmann, U.F., Hoeben, F., Forster, U., Wycisk, K., Mátyás, G., Hoyng, C.B., Riemslag, F., Meire, F., Cremers, F.P., Berger, W. Invest. Ophthalmol. Vis. Sci. (2005)
- NYX (nyctalopin on chromosome X), the gene mutated in congenital stationary night blindness, encodes a cell surface protein. Zeitz, C., Scherthan, H., Freier, S., Feil, S., Suckow, V., Schweiger, S., Berger, W. Invest. Ophthalmol. Vis. Sci. (2003)
