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Molecular genetics of Leber congenital amaurosisCREMERS, Frans P. M; VAN DEN HURK, José A. J. M; DEN HOLLANDER, Anneke I et al.Human molecular genetics (Print). 2002, Vol 11, Num 10, pp 1169-1176, issn 0964-6906Article

Novel types of mutation in the choroideremia (CHM) gene: a full-length L1 insertion and an intronic mutation activating a cryptic exonVAN DEN HURK, José A. J. M; VAN DE POL, Dorien J. R; ROPERS, Hans-Hilger et al.Human genetics. 2003, Vol 113, Num 3, pp 268-275, issn 0340-6717, 8 p.Article

Choroideremia : Variability of clinical and electrophysiological characteristics and first report of a negative electroretinogramRENNER, Agnes B; KELLNER, Ulrich; CROPP, Elke et al.Ophthalmology (Rochester, MN). 2006, Vol 113, Num 11, pp 2066-2073, issn 0161-6420, 8 p.Article

L1 retrotransposition can occur early in human embryonic developmentVAN DEN HURK, José A. J. M; MEIJ, Iwan C; DE JONG, Paulus T. V. M et al.Human molecular genetics (Print). 2007, Vol 16, Num 13, pp 1587-1592, issn 0964-6906, 6 p.Article

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