A novel TAB2 nonsense mutation (p.S149X) causing autosomal dominant congenital heart defects: a case report of a Chinese family

MLA

Jia Chen, et al. “A Novel TAB2 Nonsense Mutation (p.S149X) Causing Autosomal Dominant Congenital Heart Defects: A Case Report of a Chinese Family.” BMC Cardiovascular Disorders, vol. 20, no. 1, Jan. 2020, pp. 1–7. EBSCOhost, https://doi.org/10.1186/s12872-019-01322-1.

APA

Jia Chen, Huizhen Yuan, Kang Xie, Xinrong Wang, Linglong Tan, Yongyi Zou, Yan Yang, Lu Pan, Junfang Xiao, Ge Chen, & Yanqiu Liu. (2020). A novel TAB2 nonsense mutation (p.S149X) causing autosomal dominant congenital heart defects: a case report of a Chinese family. BMC Cardiovascular Disorders, 20(1), 1–7. https://doi.org/10.1186/s12872-019-01322-1

Chicago

Jia Chen, Huizhen Yuan, Kang Xie, Xinrong Wang, Linglong Tan, Yongyi Zou, Yan Yang, et al. 2020. “A Novel TAB2 Nonsense Mutation (p.S149X) Causing Autosomal Dominant Congenital Heart Defects: A Case Report of a Chinese Family.” BMC Cardiovascular Disorders 20 (1): 1–7. doi:10.1186/s12872-019-01322-1.