< Back to previous pageResearcher Seppe Van der AuweraerDisciplines:Molecular diagnostics, Clinical genetics and molecular diagnostics, GeneticsAffiliationsLaboratory for Neurofibromatosis Research (Division)MemberFrom1 Aug 2023 → TodayKU LeuvenProjects1 - 1 of 1Molecular and functional characterization of Legius syndrome and related disorders: Improved diagnosis and understanding of the underlying mechanisms.From1 Aug 2023 → TodayFunding: Own budget, for example: patrimony, inscription fees, giftsPublications1 - 1 of 1Encephalocraniocutaneous lipomatosis phenotype associated with mosaic biallelic pathogenic variants in the NF1 gene.(2024)Authors: Steven Smeijers, Hilde Brems, Wim Van Paesschen, Johan van Loon, Seppe Van der Auweraer, Raf Sciot, Dietmar Thal, Lieven Lagae, Eric Legius, Tom TheysPages: jmg-2023-1