Ghent University Academic Bibliography

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- Conference Paper
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Antisense oligonucleotide-based splice correction of two neighboring deep-intronic ABCA4 mutations causing Stargardt disease

Sarah Naessens, Alejandro Garanto, Miriam Bauwens (UGent) , Riccardo Sangermano, Irina Balikova (UGent) , Bart Leroy (UGent) , Frans Cremers, Elfride De Baere (UGent) and Rob Collin

(2018) Belgian Society for Human Genetics, 18th Annual meeting, Abstracts.
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- Conference Paper
- C3
Antisense oligonucleotide-based correction of deep-intronic ABCA4 splice mutations using patient-derived fibroblasts and photoreceptor precursor cells

Sarah Naessens, Alejandro Garanto, Frauke Coppieters (UGent) , Miriam Bauwens (UGent) , Irina Balikova (UGent) , Bart Leroy (UGent) , Silvia Albert, Rob Collin and Elfride De Baere (UGent)

(2018) Belgian Society for Stem Cell Research, 5th Annual meeting, Abstracts.
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- Conference Paper
- C3
Antisense oligonucleotide-based splice correction of two neighboring deep-intronic ABCA4 mutations causing Stargardt disease

Sarah Naessens, Alejandro Garanto, Miriam Bauwens (UGent) , Riccardo Sangermano, Irina Balikova (UGent) , Bart Leroy (UGent) , Frans Cremers, Elfride De Baere (UGent) and Rob Collin

(2017) European Human Genetics conference, Abstracts.
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- Conference Paper
- C3
Antisense oligonucleotide-based splice correction of two neighboring deep-intronic ABCA4 mutations causing Stargardt disease

Sarah Naessens, Alejandro Garanto, Miriam Bauwens (UGent) , Riccardo Sangermano, Irina Balikova (UGent) , Bart Leroy (UGent) , Frans Cremers, Elfride De Baere (UGent) and Rob Collin

(2017) Young Researcher Vision Camp, Abstracts.

Academic Bibliography

Antisense oligonucleotide-based splice correction of two neighboring deep-intronic ABCA4 mutations causing Stargardt disease

Antisense oligonucleotide-based correction of deep-intronic ABCA4 splice mutations using patient-derived fibroblasts and photoreceptor precursor cells

Antisense oligonucleotide-based splice correction of two neighboring deep-intronic ABCA4 mutations causing Stargardt disease

Antisense oligonucleotide-based splice correction of two neighboring deep-intronic ABCA4 mutations causing Stargardt disease

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