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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...
Autores principales: | Zaklyazminskaya, Elena, Mikhailov, Vadim, Bukaeva, Anna, Kotlukova, Natalia, Povolotskaya, Inna, Kaimonov, Vladimir, Dombrovskaya, Anna, Dzemeshkevich, Sergey |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
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 |
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