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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Publicat a:Genet Med
Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: Nature Publishing Group US 2021
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Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC8105165/
https://ncbi.nlm.nih.gov/pubmed/33500567
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41436-020-01049-x
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