MicroRNA expression profiles in familial hypertrophic cardiomyopathy with myosin-binding protein C3 (MYBPC3) gene mutations

Familial hypertrophic cardiomyopathy (FHCM) is an autosomal dominant inherited disease caused by mutations in genes encoding cardiac sarcomere proteins. MicroRNAs (miRNAs) play an important role in the pathogenesis of FHCM. In the present study, we aimed to determine the miRNA profile in FHCM patien...

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Detalles Bibliográficos
Autores principales: Lin, Li-rong, Hu, Xue-qun, Lu, Li-hong, Dai, Jia-zhen, Lin, Ning-ning, Wang, Re-hua, Xie, Zhang-xin, Chen, Xue-mei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9206743/
https://www.ncbi.nlm.nih.gov/pubmed/35717150
http://dx.doi.org/10.1186/s12872-022-02714-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9206743/
https://www.ncbi.nlm.nih.gov/pubmed/35717150
http://dx.doi.org/10.1186/s12872-022-02714-6

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