Clinical and functional characterisation of a recurrent KCNQ1 variant in the Belgian population
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Orphanet journal of rare diseases - ISSN 1750-1172-18:1 (2023) p. 1-12
Generation of a human TGFB3-hIPSC line, BBANTWi010-A, from a Loeys-Dietz syndrome type V patient
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Stem cell research - ISSN 1873-5061-65 (2022) p. 1-4
Genomics and innovative induced pluripotent stem cell (iPSC) modeling to improve understanding of pathomechanisms underlying Brugada syndrome (BrS)
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Antwerp, University of Antwerp, Faculty of Medicine and Health Sciences, Department of Medical Genetics, 2022,xvii, 234 p.
Generation of two induced pluripotent stem cell (iPSC) lines (BBANTWi006-A, BBANTWi007-A) from Brugada syndrome patients carrying an SCN5A mutation
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Stem cell research - ISSN 1873-5061-60 (2022) p. 1-4
Luminescent human iPSC-derived neurospheroids enable modeling of neurotoxicity after oxygen–glucose deprivation
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Neurotherapeutics - ISSN 1933-7213-19 (2022) p. 550-569