GRINL1A Complex Transcription Unit Containing GCOM1, MYZAP, and POLR2M Genes Associates with Fully Penetrant Recessive Dilated Cardiomyopathy

Background: Familial dilated cardiomyopathy (DCM) is a monogenic disorder typically inherited in an autosomal dominant pattern. We have identified two Finnish families with familial cardiomyopathy that is not explained by a variant in any previously known cardiomyopathy gene. We describe the cardiac...

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Detalles Bibliográficos
Autores principales: Heliö, Krista, Mäyränpää, Mikko I., Saarinen, Inka, Ahonen, Saija, Junnila, Heidi, Tommiska, Johanna, Weckström, Sini, Holmström, Miia, Toivonen, Mia, Nikus, Kjell, Hathaway, Julie, Siivonen, Pauli, Muona, Mikko, Sistonen, Johanna, Salmenperä, Pertteli, Gentile, Massimiliano, Paananen, Jussi, Myllykangas, Samuel, Alastalo, Tero-Pekka, Heliö, Tiina, Koskenvuo, Juha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8656111/
https://www.ncbi.nlm.nih.gov/pubmed/34899865
http://dx.doi.org/10.3389/fgene.2021.786705

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8656111/
https://www.ncbi.nlm.nih.gov/pubmed/34899865
http://dx.doi.org/10.3389/fgene.2021.786705

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