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.
Chicago Style CitationC., Thongnak, Limprasert P., Tangviriyapaiboon D., Silvilairat S., Puangpetch A., Pasomsub E., Sukasem C., and Chantratita W. Exome Sequencing Identifies Compound Heterozygous Mutations in SCN5A Associated With Congenital Complete Heart Block in the Thai Population. 2017.
MLA引文C., Thongnak, et al. Exome Sequencing Identifies Compound Heterozygous Mutations in SCN5A Associated With Congenital Complete Heart Block in the Thai Population. 2017.
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