C., T., P., L., D., T., S., S., A., P., E., P., . . . W., C. (2017). Exome Sequencing Identifies Compound Heterozygous Mutations in SCN5A Associated with Congenital Complete Heart Block in the Thai Population.
استشهاد بنمط شيكاغوC., Thongnak, Limprasert P., Tangviriyapaiboon D., Silvilairat S., Puangpetch A., Pasomsub E., Sukasem C., و Chantratita W. Exome Sequencing Identifies Compound Heterozygous Mutations in SCN5A Associated With Congenital Complete Heart Block in the Thai Population. 2017.
MLA استشهادC., Thongnak, et al. Exome Sequencing Identifies Compound Heterozygous Mutations in SCN5A Associated With Congenital Complete Heart Block in the Thai Population. 2017.
تحذير: قد لا تكون هذه الاستشهادات دائما دقيقة بنسبة 100%.