Identification of a nonsense mutation in TNNI3K associated with cardiac conduction disease-Reference-Cited by-同舟云学术

Identification of a nonsense mutation in TNNI3K associated with cardiac conduction disease

Published:2020-06-11 Issue:9 Volume:34 Page:
ISSN:0887-8013
Container-title:Journal of Clinical Laboratory Analysis
language:en
Short-container-title:J Clin Lab Anal

Author:

Liu Jiang¹,Liu Da¹,Li Muzheng¹,Wu Keke¹,Liu Na¹,Zhao Chenyu²,Shi Xiaoliu²³,Liu Qiming¹^ORCID

Affiliation:

1. Department of Cardiology The Second Xiangya Hospital of Central South University Changsha China

2. Department of Gastroenterology The Second Xiangya Hospital of Central South University Changsha China

3. Department of Medical Genetics The Second Xiangya Hospital of Central South University Changsha China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Microbiology (medical),Biochemistry (medical),Medical Laboratory Technology,Clinical Biochemistry,Public Health, Environmental and Occupational Health,Hematology,Immunology and Allergy

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jcla.23418

Reference25 articles.

1. Inherited progressive cardiac conduction disorders

2. Molecular and genetic insights into progressive cardiac conduction disease

3. Familial Clustering of Cardiac Conduction Defects and Pacemaker Insertion

4. 2013 ESC Guidelines on cardiac pacing and cardiac resynchronization therapy

5. Cloning and characterization of a novel cardiac-specific kinase that interacts specifically with cardiac troponin I

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