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Disease Markers
Volume 2016, Article ID 3684965, 10 pages
http://dx.doi.org/10.1155/2016/3684965
Research Article

Exome Sequencing Identifies Compound Heterozygous Mutations in SCN5A Associated with Congenital Complete Heart Block in the Thai Population

1Division of Pharmacogenomics and Personalized Medicine, Department of Pathology, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand
2Laboratory for Pharmacogenomics, Somdech Phra Debaratana Medical Center (SDMC), Ramathibodi Hospital, Bangkok, Thailand
3Excelence Center for Genomic Medicine, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand
4Human Genetics Unit, Department of Pathology, Faculty of Medicine, Prince of Songkla Univerisity, Hat Yai, Songkhla, Thailand
5Rajanagarindra Institute of Child Development, Chiang Mai, Thailand
6Division of Pediatric Cardiology, Department of Pediatrics, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand
7Virology Laboratory, Department of Pathology, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand

Received 12 July 2016; Accepted 18 October 2016

Academic Editor: Marco E. M. Peluso

Copyright © 2016 Chuphong Thongnak et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

How to Cite this Article

Chuphong Thongnak, Pornprot Limprasert, Duangkamol Tangviriyapaiboon, et al., “Exome Sequencing Identifies Compound Heterozygous Mutations in SCN5A Associated with Congenital Complete Heart Block in the Thai Population,” Disease Markers, vol. 2016, Article ID 3684965, 10 pages, 2016. https://doi.org/10.1155/2016/3684965.