Two patients with the heterozygous R189H mutation in ACTA2 and Complex congenital heart defects expands the cardiac phenotype of multisystemic smooth muscle dysfunction syndrome

DOI 10.1002/ajmg.a.38102 Am J Med Genet Part A 173A:959–965 Correspondence: Thushiha Logeswaran, M.D., Department of Pediatric Cardiology, Justus-Liebig-University of Giessen, Feulgenstraße 10-12, 35392 Gießen, Germany. Email: thushiha.logeswaran@paediat.med.uni-giessen.de The authors have brought to our attention an error in their article title. R189H should be replaced with R179H. The corrected article title follows, “Two patients with the...