Biallelic loss-of-function in NRAP is a cause of recessive dilated cardiomyopathy

BACKGROUND: Familial dilated cardiomyopathy (DCM) is typically a monogenic disorder with dominant inheritance. Although over 40 genes have been linked to DCM, more than half of the patients undergoing comprehensive genetic testing are left without molecular diagnosis. Recently, biallelic protein-tru...

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Detalles Bibliográficos
Autores principales: Koskenvuo, Juha W., Saarinen, Inka, Ahonen, Saija, Tommiska, Johanna, Weckström, Sini, Seppälä, Eija H., Tuupanen, Sari, Kangas-Kontio, Tiia, Schleit, Jennifer, Heliö, Krista, Hathaway, Julie, Gummesson, Anders, Dahlberg, Pia, Ojala, Tiina H., Vepsäläinen, Ville, Kytölä, Ville, Muona, Mikko, Sistonen, Johanna, Salmenperä, Pertteli, Gentile, Massimiliano, Paananen, Jussi, Myllykangas, Samuel, Alastalo, Tero-Pekka, Heliö, Tiina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7857588/
https://www.ncbi.nlm.nih.gov/pubmed/33534821
http://dx.doi.org/10.1371/journal.pone.0245681

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7857588/
https://www.ncbi.nlm.nih.gov/pubmed/33534821
http://dx.doi.org/10.1371/journal.pone.0245681

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