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) - Forschungsportal der Justus-Liebig-Universität Gießen:

Journalartikel

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)

Autorenliste: 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

Jahr der Veröffentlichung: 2017

Seiten: 2566-2566

Zeitschrift: The American Journal of Medical Genetics - Part A

Bandnummer: 173

Heftnummer: 9

ISSN: 1552-4825

eISSN: 1552-4833

Open Access Status: Bronze

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

Verlag: Wiley

Zitierstile

Harvard-Zitierstil: 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-Zitierstil: 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

Nachhaltigkeitsbezüge

3 Gesundheit und Wohlergehen