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

BACKGROUND: Cardiac conduction disease (CCD) is a common cardiovascular disease which can lead to life‐threatening conditions. The importance of heredity in CCD has been realized in recent years. Several causal genes have been found to be implicated in CCD such as SCN5A, TRPM4, SCN1B, TNNI3K, LMNA,...

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Detalles Bibliográficos
Autores principales: Liu, Jiang, Liu, Da, Li, Muzheng, Wu, Keke, Liu, Na, Zhao, Chenyu, Shi, Xiaoliu, Liu, Qiming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7521241/
https://www.ncbi.nlm.nih.gov/pubmed/32529721
http://dx.doi.org/10.1002/jcla.23418

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7521241/
https://www.ncbi.nlm.nih.gov/pubmed/32529721
http://dx.doi.org/10.1002/jcla.23418

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