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Journal of Translational Medicine logoLink to Journal of Translational Medicine
. 2017 May 11;15:101. doi: 10.1186/s12967-017-1203-y

Erratum to: Novel trigenic CACNA1C/DES/MYPN mutations in a family of hypertrophic cardiomyopathy with early repolarization and short QT syndrome

Yanhong Chen 1,2, Hector Barajas‑Martinez 4, Dongxiao Zhu 2, Xihui Wang 2, Chonghao Chen 2, Ruijuan Zhuang 2, Jingjing Shi 2, Xueming Wu 2, Yijia Tao 2, Weidong Jin 2, Xiaoyan Wang 2,, Dan Hu 3,4,5,
PMCID: PMC5425985  PMID: 28490369

Erratum to: J Transl Med (2017) 15:78 DOI 10.1186/s12967-017-1180-1

In the original publication of this article [1], Figure 2 is incorrect. In this Erratum the original figure (Fig. 1) and the correct figure (Fig. 2) are published.

Fig. 1.

Fig. 1

Original version of Fig. 2 as published on 20 April 2017

Fig. 2.

Fig. 2

Corrected version of Figure 2; panel b has been updated

Acknowledgments

Publisher's Note

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Footnotes

The online version of the original article can be found under doi:10.1186/s12967-017-1180-1.

Contributor Information

Xiaoyan Wang, Email: 1807250234@qq.com.

Dan Hu, Email: dianah@mmrl.edu.

Reference

  • 1.Chen Y, Barajas-Martinez H, Zhu D, Wang X, Chen C, Zhuang R, Shi J, Wu X, Tao Y, Jin W, Wang X, Hu D. Novel trigenic CACNA1C/DES/MYPN mutations in a family of hypertrophic cardiomyopathy with early repolarization and short QT syndrome. J Transl Med. 2017;18:81. doi: 10.1186/s12967-017-1180-1. [DOI] [PMC free article] [PubMed] [Google Scholar]

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