Clinical and functional characterisation of a recurrent KCNQ1 variant in the Belgian population
Source
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
Source
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)
Source
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
Source
Stem cell research - ISSN 1873-5061-60 (2022) p. 1-4
Luminescent human iPSC-derived neurospheroids enable modeling of neurotoxicity after oxygen–glucose deprivation
Source
Neurotherapeutics - ISSN 1933-7213-19 (2022) p. 550-569