Case Report: Two New Cases of Autosomal-Recessive Hypertrophic Cardiomyopathy Associated With TRIM63-Compound Heterozygous Variant

Hypertrophic cardiomyopathy (HCM) is one of the most common hereditary diseases, and it is associated with fatal complications. The clinical heterogeneity of HCM requires risk prediction models to identify patients at a high risk of adverse events. Most HCM cases are caused by mutations in genes enc...

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Detalles Bibliográficos
Autores principales: Andreeva, Sofiya, Chumakova, Olga, Karelkina, Elena, Lebedeva, Viktoriya, Lubimtseva, Tamara, Semenov, Andrey, Nikitin, Alexey, Speshilov, Gleb, Kozyreva, Alexandra, Sokolnikova, Polina, Zhuk, Sergey, Fomicheva, Yuliya, Moiseeva, Olga, Kostareva, Anna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8901572/
https://www.ncbi.nlm.nih.gov/pubmed/35273634
http://dx.doi.org/10.3389/fgene.2022.743472

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8901572/
https://www.ncbi.nlm.nih.gov/pubmed/35273634
http://dx.doi.org/10.3389/fgene.2022.743472

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