Diagnostic yield of genetic testing in a multinational heterogeneous cohort of 2088 DCM patients

BACKGROUND: Familial dilated cardiomyopathy (DCM) causes heart failure and may lead to heart transplantation. DCM is typically a monogenic disorder with autosomal dominant inheritance. Currently disease-causing variants have been reported in over 60 genes that encode proteins in sarcomeres, nuclear...

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Detalles Bibliográficos
Autores principales: Heliö, Krista, Cicerchia, Marcos, Hathaway, Julie, Tommiska, Johanna, Huusko, Johanna, Saarinen, Inka, Koskinen, Lotta, Muona, Mikko, Kytölä, Ville, Djupsjöbacka, Janica, Gentile, Massimiliano, Salmenperä, Pertteli, Alastalo, Tero-Pekka, Steinberg, Christian, Heliö, Tiina, Paananen, Jussi, Myllykangas, Samuel, Koskenvuo, Juha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Cardiovascular Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10546047/
https://www.ncbi.nlm.nih.gov/pubmed/37795486
http://dx.doi.org/10.3389/fcvm.2023.1254272

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10546047/
https://www.ncbi.nlm.nih.gov/pubmed/37795486
http://dx.doi.org/10.3389/fcvm.2023.1254272

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