APA استشهاد

Walklate, J., Vera, C., Bloemink, M. J., Geeves, M. A., & Leinwand, L. (2016). The Most Prevalent Freeman-Sheldon Syndrome Mutations in the Embryonic Myosin Motor Share Functional Defects. J Biol Chem.

استشهاد بنمط شيكاغو

Walklate, Jonathan, Carlos Vera, Marieke J. Bloemink, Michael A. Geeves, و Leslie Leinwand. "The Most Prevalent Freeman-Sheldon Syndrome Mutations in the Embryonic Myosin Motor Share Functional Defects." J Biol Chem 2016.

MLA استشهاد

Walklate, Jonathan, et al. "The Most Prevalent Freeman-Sheldon Syndrome Mutations in the Embryonic Myosin Motor Share Functional Defects." J Biol Chem 2016.

تحذير: قد لا تكون هذه الاستشهادات دائما دقيقة بنسبة 100%.