Systematic large-scale assessment of the genetic architecture of left ventricular noncompaction reveals diverse etiologies

PURPOSE: To characterize the genetic architecture of left ventricular noncompaction (LVNC) and investigate the extent to which it may represent a distinct pathology or a secondary phenotype associated with other cardiac diseases. METHODS: We performed rare variant association analysis with 840 LVNC...

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Detalles Bibliográficos
Autores principales: Mazzarotto, Francesco, Hawley, Megan H., Beltrami, Matteo, Beekman, Leander, de Marvao, Antonio, McGurk, Kathryn A., Statton, Ben, Boschi, Beatrice, Girolami, Francesca, Roberts, Angharad M., Lodder, Elisabeth M., Allouba, Mona, Romeih, Soha, Aguib, Yasmine, Baksi, A. John, Pantazis, Antonis, Prasad, Sanjay K., Cerbai, Elisabetta, Yacoub, Magdi H., O’Regan, Declan P., Cook, Stuart A., Ware, James S., Funke, Birgit, Olivotto, Iacopo, Bezzina, Connie R., Barton, Paul J. R., Walsh, Roddy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8105165/
https://www.ncbi.nlm.nih.gov/pubmed/33500567
http://dx.doi.org/10.1038/s41436-020-01049-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8105165/
https://www.ncbi.nlm.nih.gov/pubmed/33500567
http://dx.doi.org/10.1038/s41436-020-01049-x

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