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TAB2 deletions and variants cause a highly recognisable syndrome with mitral valve disease, cardiomyopathy, short stature and hypermobility

Aafke Engwerda, Erika Leenders, Barbara Frentz, Paulien A. Terhal, Katharina Löhner, Bert B.A. de Vries, Trijnie Dijkhuizen, Yvonne J. Vos, Tuula Rinne, Maarten P. van den Berg, M. T. R. Roofthooft, Patrick Deelen, Conny M.A. van Ravenswaaij‐Arts, Wilhelmina S. Kerstjens‐Frederikse

2021European Journal of Human Genetics31 citationsDOIOpen Access PDF

Topics & Concepts

HaploinsufficiencyShort statureNoonan syndromeCardiomyopathyPhenotypeMitral valve prolapseGeneticsDiseaseGenetic heterogeneityMedicineHeart failureInternal medicineBiologyMitral valveGeneProtein Tyrosine PhosphatasesPeptidase Inhibition and AnalysisRNA modifications and cancer
TAB2 deletions and variants cause a highly recognisable syndrome with mitral valve disease, cardiomyopathy, short stature and hypermobility | Litcius