Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease
(2019) Stijn Van De Sompele (UGent), Claire Smith, Marianthi Karali, Marta Corton, Kristof Van Schil (UGent), Frank Peelman (UGent), Timothy Cherry, Toon Rosseel (UGent), Hannah Verdin (UGent), Julien Derolez (UGent), Thalia Van Laethem (UGent), Kamron N. Khan, Martin McKibbin, Carmel Toomes, Manir Ali, Annalaura Torella, Francesco Testa, Francesca Simonelli, Julie De Zaeytijd (UGent), Jenneke Van den Ende, Bart Leroy (UGent), Frauke Coppieters (UGent), Carmen Ayuso, Chris F Inglehearn, Sandro Banfi, Elfride De Baere (UGent)
Antisense oligonucleotide-based downregulation of the G56R pathogenic variant causing NR2E3-associated autosomal dominant retinitis pigmentosa
(2019) Sarah Naessens (UGent), Laurien Ruysschaert (UGent), Steve Lefever (UGent), Frauke Coppieters (UGent), Elfride De Baere (UGent)
Antisense oligonucleotide-based splice correction of two neighboring deep-intronic ABCA4 mutations causing Stargardt disease
(2018) Sarah Naessens (UGent), Alejandro Garanto, Miriam Bauwens (UGent), Riccardo Sangermano, Irina Balikova (UGent), Bart Leroy (UGent), Frans Cremers, Elfride De Baere (UGent), Rob Collin
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