Publications by authors named "Rob Wj Collin"

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Gene augmentation of LCA5-associated Leber congenital amaurosis ameliorates bulge region defects of the photoreceptor ciliary axoneme.
Siebren Faber, Olivier Mercey, Katrin Junger, Alejandro Garanto, Helen May-Simera, Rob Wj Collin

JCI Insight· May 2023

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Antisense Oligonucleotide-based Splice Correction for USH2A-associated Retinal Degeneration Caused by a Frequent Deep-intronic Mutation.
Radulfus Wn Slijkerman, Christel Vaché, Margo Dona, Gema García-García, Mireille Claustres, Rob Wj Collin

Mol Ther Nucleic Acids· November 2016

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Autosomal recessive retinitis pigmentosa with RP1 mutations is associated with myopia.
Thomas Chassine, Béatrice Bocquet, Vincent Daien, Almudena Avila-Fernandez, Carmen Ayuso, Rob Wj Collin

Br J Ophthalmol· October 2015

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Antisense Oligonucleotide (AON)-based Therapy for Leber Congenital Amaurosis Caused by a Frequent Mutation in CEP290.
Rob Wj Collin, Anneke I den Hollander, Saskia D van der Velde-Visser, Jeannette Bennicelli, Jean Bennett

Mol Ther Nucleic Acids· March 2012

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