Copy number variants in Ebstein anomaly

BACKGROUND: Ebstein anomaly (EA) is a rare congenital defect characterized by apical displacement of the septal tricuspid leaflets and atrialization of the right ventricle. The etiology of EA is unclear; however, recurrence in families and the association of EA with genetic syndromes and copy number...

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Pubblicato in:PLoS One
Autori principali: Giannakou, Andreas, Sicko, Robert J., Zhang, Wei, Romitti, Paul, Browne, Marilyn L., Caggana, Michele, Brody, Lawrence C., Jelliffe-Pawlowski, Laura, Shaw, Gary M., Kay, Denise M., Mills, James L.
Natura: Artigo
Lingua:Inglês
Pubblicazione: Public Library of Science 2017
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Research Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC5720705/
https://ncbi.nlm.nih.gov/pubmed/29216221
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0188168
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