A novel TBX20 loss-of-function mutation contributes to adult-onset dilated cardiomyopathy or congenital atrial septal defect.

MLA

Yi-Meng Zhou, et al. “A Novel TBX20 Loss-of-Function Mutation Contributes to Adult-Onset Dilated Cardiomyopathy or Congenital Atrial Septal Defect.” Molecular Medicine Reports, vol. 14, no. 4, Oct. 2016, pp. 3307–14. EBSCOhost, https://doi.org/10.3892/mmr.2016.5609.

APA

Yi-Meng Zhou, Xiao-Yong Dai, Ri-Tai Huang, Song Xue, Ying-Jia Xu, Xing-Biao Qiu, & Yi-Qing Yang. (2016). A novel TBX20 loss-of-function mutation contributes to adult-onset dilated cardiomyopathy or congenital atrial septal defect. Molecular Medicine Reports, 14(4), 3307–3314. https://doi.org/10.3892/mmr.2016.5609

Chicago

Yi-Meng Zhou, Xiao-Yong Dai, Ri-Tai Huang, Song Xue, Ying-Jia Xu, Xing-Biao Qiu, and Yi-Qing Yang. 2016. “A Novel TBX20 Loss-of-Function Mutation Contributes to Adult-Onset Dilated Cardiomyopathy or Congenital Atrial Septal Defect.” Molecular Medicine Reports 14 (4): 3307–14. doi:10.3892/mmr.2016.5609.