RE, N., RM, G., AA, E., AA, K., AF, E., & M, E. (2026). Whole-exome sequencing identifies rare genetic variants in Egyptian patients with hypertrophic cardiomyopathy: A pilot study. Cardiology in the young, 1. https://doi.org/10.1017/S1047951126123622
Chicago Style (17th ed.) CitationRE, Negm, Gabre RM, El-Sherif AA, Katta AA, El-Sayed AF, and ElHefnawi M. "Whole-exome Sequencing Identifies Rare Genetic Variants in Egyptian Patients with Hypertrophic Cardiomyopathy: A Pilot Study." Cardiology in the Young 2026: 1. https://doi.org/10.1017/S1047951126123622.
MLA (9th ed.) CitationRE, Negm, et al. "Whole-exome Sequencing Identifies Rare Genetic Variants in Egyptian Patients with Hypertrophic Cardiomyopathy: A Pilot Study." Cardiology in the Young, 2026, p. 1, https://doi.org/10.1017/S1047951126123622.