APA استشهاد

Thongnak, C., Limprasert, P., Tangviriyapaiboon, D., Silvilairat, S., Puangpetch, A., Pasomsub, E., . . . Chantratita, W. (2018). Exome Sequencing Identifies Compound Heterozygous Mutations in SCN5A Associated with Congenital Complete Heart Block in the Thai Population.

استشهاد بنمط شيكاغو

Thongnak, Chuphong, Pornprot Limprasert, Duangkamol Tangviriyapaiboon, Suchaya Silvilairat, Apichaya Puangpetch, Ekawat Pasomsub, Chonlaphat Sukasem, و Wasun Chantratita. Exome Sequencing Identifies Compound Heterozygous Mutations in SCN5A Associated With Congenital Complete Heart Block in the Thai Population. 2018.

MLA استشهاد

Thongnak, Chuphong, et al. Exome Sequencing Identifies Compound Heterozygous Mutations in SCN5A Associated With Congenital Complete Heart Block in the Thai Population. 2018.

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