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Impact of Troponin in Cardiomyopathy Development Caused by Mutations in Tropomyosin

Tropomyosin (Tpm) mutations cause inherited cardiac diseases such as hypertrophic and dilated cardiomyopathies. We applied various approaches to investigate the role of cardiac troponin (Tn) and especially the troponin T (TnT) in the pathogenic effects of Tpm cardiomyopathy-associated mutations M8R,...

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Detalles Bibliográficos
Autores principales:	Nefedova, Victoria V., Kopylova, Galina V., Shchepkin, Daniil V., Kochurova, Anastasia M., Kechko, Olga I., Borzova, Vera A., Ryabkova, Natalia S., Katrukha, Ivan A., Mitkevich, Vladimir A., Bershitsky, Sergey Y., Levitsky, Dmitrii I., Matyushenko, Alexander M.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2022
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9779223/ https://www.ncbi.nlm.nih.gov/pubmed/36555368 http://dx.doi.org/10.3390/ijms232415723

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