Samudrala, S. S. K., North, L. M., Stamm, K. D., Earing, M. G., Frommelt, M. A., Willes, R., . . . Tomita‐Mitchell, A. (2020). Novel KLHL26 variant associated with a familial case of Ebstein’s anomaly and left ventricular noncompaction. Mol Genet Genomic Med.
Chicago ZitierstilSamudrala, Sai Suma K., et al. "Novel KLHL26 Variant Associated With a Familial Case of Ebstein’s Anomaly and Left Ventricular Noncompaction." Mol Genet Genomic Med 2020.
MLA ZitierstilSamudrala, Sai Suma K., et al. "Novel KLHL26 Variant Associated With a Familial Case of Ebstein’s Anomaly and Left Ventricular Noncompaction." Mol Genet Genomic Med 2020.
Achtung: Diese Zitate sind unter Umständen nicht zu 100% korrekt.