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
Topics & Concepts
HaploinsufficiencyShort statureNoonan syndromeCardiomyopathyPhenotypeMitral valve prolapseGeneticsDiseaseGenetic heterogeneityMedicineHeart failureInternal medicineBiologyMitral valveGeneProtein Tyrosine PhosphatasesPeptidase Inhibition and AnalysisRNA modifications and cancer