Mutation profile of FLNC gene and its prognostic relevance in patients with hypertrophic cardiomyopathy

BACKGROUND: Filamin C (FLNC) mutation was reported as a cause of HCM, with a high probability of sudden cardiac death. However, the mutation profile of FLNC, and its relationship with phenotypic expression in HCM, remains to be elucidated. METHODS: In this study, FLNC gene was sequenced in 540 HCM p...

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Shranjeno v:
Bibliografske podrobnosti
izdano v:Mol Genet Genomic Med
Main Authors: Cui, Hao, Wang, Jizheng, Zhang, Ce, Wu, Guixin, Zhu, Changsheng, Tang, Bing, Zou, Yubao, Huang, Xiaohong, Hui, Rutai, Song, Lei, Wang, Shuiyun
Format: Artigo
Jezik:Inglês
Izdano: John Wiley and Sons Inc. 2018
Teme:
Original Articles
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC6305649/
https://ncbi.nlm.nih.gov/pubmed/30411535
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.488
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