Showing results (1-10 of 5) with videos related to
Sort By:
Pageof 1
Human Molecular Genetics|August 9, 2023
Stargardt disease-associated missense and synonymous ABCA4 variants result in aberrant splicingMelita Kaltak, Zelia Corradi, Rob W J Collin, et al.Scientific Reports|January 5, 2024
QR-1011 restores defective ABCA4 splicing caused by multiple severe ABCA4 variants underlying Stargardt diseaseMelita Kaltak, Petra de Bruijn, Willemijn van Leeuwen, et al.Clinical Chemistry|August 21, 2020
Ultrasensitive DNA Immune Repertoire Sequencing Using Unique Molecular IdentifiersGustav Johansson, Melita Kaltak, Cristiana Rîmniceanu, et al.Journal of Translational Medicine|August 16, 2023
Stargardt disease-associated in-frame ABCA4 exon 17 skipping results in significant ABCA4 functionMelita Kaltak, Rocio Blanco-Garavito, Laurie L Molday, et al.Molecular Therapy. Nucleic Acids|March 13, 2023
Antisense oligonucleotide therapy corrects splicing in the common Stargardt disease type 1-causing variant ABCA4 c.5461-10T>CMelita Kaltak, Petra de Bruijn, Davide Piccolo, et al.Pageof 1