Whole-genome sequencing identifies novel candidate pathogenic variants associated with left ventricular non-compaction in a three-generation family

Clin Transl Med. 2021 Aug;11(8):e501. doi: 10.1002/ctm2.501.

Authors

Zhe Zhang¹, Shiying Li², Kun Wang¹, Zicheng Zhao², Heng Zhang³, Shuaicheng Li⁴, Xiaofei Jiang¹

Affiliations

¹ Department of Cardiology, Zhuhai People's Hospital (Zhuhai Hospital Affiliated with Jinan University), Zhuhai, Guangdong, P. R. China.
² Shenzhen Byoryn Technology Co., Ltd, Shenzhen, Guangdong, P. R. China.
³ Department of Ultrasonography, Zhuhai People's Hospital (Zhuhai Hospital Affiliated with Jinan University), Zhuhai, Guangdong, P. R. China.
⁴ Shenzhen Research Institute, City University of Hong Kong, Shenzhen, Guangdong, P. R. China.

No abstract available

Publication types

Letter
Research Support, Non-U.S. Gov't

MeSH terms

Child
China
Echocardiography / methods
Female
Heart Defects, Congenital / diagnostic imaging*
Heart Defects, Congenital / genetics*
Heart Ventricles / diagnostic imaging
Humans
Male
Middle Aged
Whole Genome Sequencing / methods*

Supplementary concepts

Noncompaction of Left Ventricular Myocardium with Congenital Heart Defects

Grants and funding

Zhuhai People's Hospital