CNGA3 mutations in hereditary cone photoreceptor disorders

Publication year
2001
Author(s)
Wissinger, B.
Gamer, D.
Jagle, H.
Giorda, R.
Marx, T.
Mayer, S.
Tippmann, S.
Broghammer, M.
Jurklies, B.
Rosenberg, T.
Jacobson, S.G.
Sener, E.C.
Tatlipinar, S.
Hoyng, C.B.
Castellan, C.
Bitoun, P.
Andreasson, S.
Rudolph, G.
Kellner, U.
Lorenz, B.
Wolff, G.
Verellen-Dumoulin, C.
Schwartz, M.
Cremers, F.P.M.
Apfelstedt-Sylla, E.
Zrenner, E.
Salati, R.
Sharpe, L.T.
Kohl, S.
Source
American Journal of Human Genetics, 69, 4, (2001), pp. 722-737
ISSN
DOI
Publication type
Article / Letter to editor
Please use this identifier to cite or link to this item: https://hdl.handle.net/2066/142520   https://hdl.handle.net/2066/142520
Display more details

Upload full text

Use your RU credentials (u/z-number and password) to log in with SURFconext to upload a file for processing by the repository team.