The 2588G -> C mutation in the ABCR gene is a mild frequent founder mutation in the western European population and allows the classification of ABCR mutations in patients with Stargardt disease.

Publication year
1999
Author(s)
Maugeri, A.
Driel, M.A. van
Pol, T.J.R. van de
Klevering, B.J.
Haren, F.J.J. van
Tijmes, N.
Bergen, A.A.B.
Rohrschneider, K.
Blankenagel, A.
Pinckers, A.J.L.G.
Dahl, N.
Brunner, H.G.
Deutman, A.F.
Hoyng, C.B.
Cremers, F.P.M.
Source
American Journal of Human Genetics, 64, (1999), pp. 1024-1035
ISSN
DOI
Publication type
Article / Letter to editor
Please use this identifier to cite or link to this item: https://hdl.handle.net/2066/143939   https://hdl.handle.net/2066/143939
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