Low mutation rate in the TTN gene in paediatric patients with dilated cardiomyopathy – a pilot study

Idiopathic dilated cardiomyopathy (DCM) is a common cardiomyopathy with the prevalence of 1:250, and at least one-third of all the cases are inherited. Mutations in the TTN gene are considered as the most frequent cause of inherited DCM and cover 10–30% of the cases. The studies were mainly focused...

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Detalles Bibliográficos
Autores principales: Zaklyazminskaya, Elena, Mikhailov, Vadim, Bukaeva, Anna, Kotlukova, Natalia, Povolotskaya, Inna, Kaimonov, Vladimir, Dombrovskaya, Anna, Dzemeshkevich, Sergey
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6848193/
https://www.ncbi.nlm.nih.gov/pubmed/31712709
http://dx.doi.org/10.1038/s41598-019-52911-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6848193/
https://www.ncbi.nlm.nih.gov/pubmed/31712709
http://dx.doi.org/10.1038/s41598-019-52911-1

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