A novel nonsense mutation in TNNT2 in a Chinese pedigree with hypertrophic cardiomyopathy: A case report

RATIONALE: Hypertrophic cardiomyopathy (HCM) is an inherited myocardial disease and a common cause of sudden cardiac death, heart failure, atrial fibrillation and stroke. In families affected by HCM, genotyping is useful for identifying susceptible relatives. In the present study, we investigated th...

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Detalles Bibliográficos
Autores principales: Gao, Guangyuan, Liu, Guohui, Chen, Weiwei, Tong, Yaliang, Mao, Cuiying, Liu, Jinsha, Zhang, Xing, He, Max M., Yang, Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2020
Materias:
3400
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7447477/
https://www.ncbi.nlm.nih.gov/pubmed/32846832
http://dx.doi.org/10.1097/MD.0000000000021843

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7447477/
https://www.ncbi.nlm.nih.gov/pubmed/32846832
http://dx.doi.org/10.1097/MD.0000000000021843

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