Novel mutations of TCTN3/LTBP2 with cellular function changes in congenital heart disease associated with polydactyly-Reference-Cited by-同舟云学术

Novel mutations of TCTN3/LTBP2 with cellular function changes in congenital heart disease associated with polydactyly

Published:2020-10-24 Issue:23 Volume:24 Page:13751-13762
ISSN:1582-1838
Container-title:Journal of Cellular and Molecular Medicine
language:en
Short-container-title:J. Cell. Mol. Med.

Author:

Chen Huan‐Xin¹,Yang Zi‐Yue²,Hou Hai‐Tao¹,Wang Jun¹,Wang Xiu‐Li¹,Yang Qin¹,Liu Lin²,He Guo‐Wei¹³⁴⁵^ORCID

Affiliation:

1. Center for Basic Medical Research & Department of Cardiovascular Surgery TEDA International Cardiovascular Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College Tianjin China

2. College of Life Sciences Nankai University Tianjin China

3. Zhejiang University Hangzhou Zhejiang China

4. Drug Research and Development Center Wannan Medical College Wuhu Anhui China

5. Department of Surgery Oregon Health and Science University Portland OR USA

Funder

National Natural Science Foundation of China

Chinese Academy of Medical Sciences

Publisher

Wiley

Subject

Cell Biology,Molecular Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/jcmm.15950

Reference29 articles.

1. Birth Prevalence of Congenital Heart Disease Worldwide

2. Advances in the Understanding of the Genetic Determinants of Congenital Heart Disease and Their Impact on Clinical Outcomes

3. Variation in Outcomes for Benchmark Operations: An Analysis of The Society of Thoracic Surgeons Congenital Heart Surgery Database

4. Identification of a novel and functional mutation in the TBX5 gene in a patient by screening from 354 patients with isolated ventricular septal defect

5. A Novel Variation of PLAGL1 in Chinese Patients with Isolated Ventricular Septal Defect

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