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 CitationC., Thongnak, et al. Exome Sequencing Identifies Compound Heterozygous Mutations in SCN5A Associated With Congenital Complete Heart Block in the Thai Population. 2017.
Warning: These citations may not always be 100% accurate.