Clinical Significance of Variants in the TTN Gene in a Large Cohort of Patients With Sporadic Dilated Cardiomyopathy

Background: Mutations in the TTN gene are the most common causes of dilated cardiomyopathy (DCM). The clinical significance of TTN gene variants remains inadequately understood. Methods: Whole-exome sequencing and phenotypic characterisation were performed, and patients were followed up for a median...

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Detalles Bibliográficos
Autores principales: Xiao, Lei, Li, Chenze, Sun, Yang, Chen, Yanghui, Wei, Haoran, Hu, Dong, Yu, Ting, Li, Xianqing, Jin, Li, Shi, Leming, Marian, Ali J., Wang, Dao Wen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Cardiovascular Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8120103/
https://www.ncbi.nlm.nih.gov/pubmed/33996946
http://dx.doi.org/10.3389/fcvm.2021.657689

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8120103/
https://www.ncbi.nlm.nih.gov/pubmed/33996946
http://dx.doi.org/10.3389/fcvm.2021.657689

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