APA (7th ed.) Citation

Kraoua, L., Jaouadi, H., Allouche, M., Achour, A., Kaouther, H., Ahmed, H. B., . . . M'rad, R. (2022). Molecular autopsy and clinical family screening in a case of sudden cardiac death reveals ACTN2 mutation related to hypertrophic/dilated cardiomyopathy and a novel LZTR1 variant associated with Noonan syndrome. Molecular Genetics & Genomic Medicine, 10(7), 1. https://doi.org/10.1002/mgg3.1954

Chicago Style (17th ed.) Citation

Kraoua, Lilia, et al. "Molecular Autopsy and Clinical Family Screening in a Case of Sudden Cardiac Death Reveals ACTN2 Mutation Related to Hypertrophic/dilated Cardiomyopathy and a Novel LZTR1 Variant Associated with Noonan Syndrome." Molecular Genetics & Genomic Medicine 10, no. 7 (2022): 1. https://doi.org/10.1002/mgg3.1954.

MLA (9th ed.) Citation

Kraoua, Lilia, et al. "Molecular Autopsy and Clinical Family Screening in a Case of Sudden Cardiac Death Reveals ACTN2 Mutation Related to Hypertrophic/dilated Cardiomyopathy and a Novel LZTR1 Variant Associated with Noonan Syndrome." Molecular Genetics & Genomic Medicine, vol. 10, no. 7, 2022, p. 1, https://doi.org/10.1002/mgg3.1954.