Ceznerová, E.; Kaufmanová, J.; Sovová, Ž.; Å tikarová, J.; Loužil, J.; KotlÃn, R.; Suttnar, J.
Structural and Functional Characterization of Four Novel Fibrinogen Mutations in FGB Causing Congenital Fibrinogen Disorder. Int. J. Mol. Sci. 2022, 23, 721.
https://doi.org/10.3390/ijms23020721
AMA Style
Ceznerová E, Kaufmanová J, Sovová Ž, Å tikarová J, Loužil J, KotlÃn R, Suttnar J.
Structural and Functional Characterization of Four Novel Fibrinogen Mutations in FGB Causing Congenital Fibrinogen Disorder. International Journal of Molecular Sciences. 2022; 23(2):721.
https://doi.org/10.3390/ijms23020721
Chicago/Turabian Style
Ceznerová, EliÅ¡ka, JiÅ™ina Kaufmanová, Žofie Sovová, Jana Å tikarová, Jan Loužil, Roman KotlÃn, and Jiřà Suttnar.
2022. "Structural and Functional Characterization of Four Novel Fibrinogen Mutations in FGB Causing Congenital Fibrinogen Disorder" International Journal of Molecular Sciences 23, no. 2: 721.
https://doi.org/10.3390/ijms23020721
APA Style
Ceznerová, E., Kaufmanová, J., Sovová, Ž., Å tikarová, J., Loužil, J., KotlÃn, R., & Suttnar, J.
(2022). Structural and Functional Characterization of Four Novel Fibrinogen Mutations in FGB Causing Congenital Fibrinogen Disorder. International Journal of Molecular Sciences, 23(2), 721.
https://doi.org/10.3390/ijms23020721