Two patients with the heterozygous R189H mutation in <i>ACTA2</i> and Complex congenital heart defects expands the cardiac phenotype of multisystemic smooth muscle dysfunction syndrome (vol 173, pg 959, 2017) - Research portal of Justus Liebig University Giessen:

Journal article

Two patients with the heterozygous R189H mutation in ACTA2 and Complex congenital heart defects expands the cardiac phenotype of multisystemic smooth muscle dysfunction syndrome (vol 173, pg 959, 2017)

Authors list: Logeswaran, Thushiha; Friedburg, Christoph; Hofmann, Karoline; Akintuerk, Hakan; Biskup, Saskia; Graef, Michael; Rad, Ali; Weber, Axel; Neubauer, Bernd A.; Schranz, Dietmar; Bouvagnet, Patrice; Lorenz, Birgit; Hahn, Andreas

Publication year: 2017

Pages: 2566-2566

Journal: The American Journal of Medical Genetics - Part A

Volume number: 173

Issue number: 9

ISSN: 1552-4825

eISSN: 1552-4833

Open access status: Bronze

DOI Link: https://doi.org/10.1002/ajmg.a.38329

Publisher: Wiley

Citation Styles

Harvard Citation style: Logeswaran, T., Friedburg, C., Hofmann, K., Akintuerk, H., Biskup, S., Graef, M., et al. (2017) Two patients with the heterozygous R189H mutation in ACTA2 and Complex congenital heart defects expands the cardiac phenotype of multisystemic smooth muscle dysfunction syndrome (vol 173, pg 959, 2017), The American Journal of Medical Genetics - Part A, 173(9), p. 2566. https://doi.org/10.1002/ajmg.a.38329

APA Citation style: Logeswaran, T., Friedburg, C., Hofmann, K., Akintuerk, H., Biskup, S., Graef, M., Rad, A., Weber, A., Neubauer, B., Schranz, D., Bouvagnet, P., Lorenz, B., & Hahn, A. (2017). Two patients with the heterozygous R189H mutation in ACTA2 and Complex congenital heart defects expands the cardiac phenotype of multisystemic smooth muscle dysfunction syndrome (vol 173, pg 959, 2017). The American Journal of Medical Genetics - Part A. 173(9), 2566. https://doi.org/10.1002/ajmg.a.38329

SDG Areas

3 Good health and well-being