The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein

Publication year
2000
Author(s)
Pusch, C.M.
Zeitz, C.
Brandau, O.
Pesch, K.
Achatz, H.
Feil, S.
Scharfe, C.
Maurer, J.
Jacobi, F.K.
Pinckers, A.J.L.G.
Andreasson, S.
Hardcastle, A.
Wissinger, B.
Berger, W.
Meindle, A.
Source
Nature Genetics, 26, 3, (2000), pp. 324-327
ISSN
DOI
Publication type
Article / Letter to editor
Please use this identifier to cite or link to this item: https://hdl.handle.net/2066/184658   https://hdl.handle.net/2066/184658
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.