Autosomal recessive retinitis pigmentosa and cone-rod dystrophy caused by splice site mutations in the Stargardt's disease gene ABCR

Publication year
1998
Author(s)
Cremers, F.P.M.
Pol, T.J.R. van de
Driel, M.A. van
Hollander, A.I. den
Haren, F.J.J. van
Knoers, N.V.A.M.
Tijmes, N.
Bergen, A.A.B.
Rohrschneider, K.
Blankenagel, A.
Pinckers, A.J.L.G.
Deutman, A.F.
Hoyng, C.B.
Number of pages
8 p.
Source
Human Molecular Genetics, 7, (1998), pp. 355-362
ISSN
Publication type
Article / Letter to editor
If a DOI or any other persistent identifier is unavailable, please use the following repository identifier to link to this item: https://hdl.handle.net/2066/134236   https://hdl.handle.net/2066/134236
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