APA استشهاد

Matsumura, H., Nakano, Y., Ochi, H., Onohara, Y., Sairaku, A., Tokuyama, T., . . . Kihara, Y. (2017). H558R, a common SCN5A polymorphism, modifies the clinical phenotype of Brugada syndrome by modulating DNA methylation of SCN5A promoters. J Biomed Sci.

استشهاد بنمط شيكاغو

Matsumura, Hiroya, et al. "H558R, a Common SCN5A Polymorphism, Modifies the Clinical Phenotype of Brugada Syndrome By Modulating DNA Methylation of SCN5A Promoters." J Biomed Sci 2017.

MLA استشهاد

Matsumura, Hiroya, et al. "H558R, a Common SCN5A Polymorphism, Modifies the Clinical Phenotype of Brugada Syndrome By Modulating DNA Methylation of SCN5A Promoters." J Biomed Sci 2017.

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