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Thr-4-Lys rhodopsin mutation is associated with autosomal dominant retinitis pigmentosa of the cone-rod type in a small Dutch family

Born, L.I. van den and Schooneveld, M.J. van and Jong, L.A.M.S. de and Riemslag, F.C.C. and Jong de, P.T.V.M. and Gal, A. and Bleeker-Wagemakers, E.M. (1994) Thr-4-Lys rhodopsin mutation is associated with autosomal dominant retinitis pigmentosa of the cone-rod type in a small Dutch family. Ophthalmic genetics, 15, 51-60. ISSN 13816810.

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Item Type:Article
Institutes:Netherlands Institute for Neuroscience (NIN)
ID Code:1542
Deposited On:13 Feb 2009 16:58
Last Modified:13 Oct 2010 22:32

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