Novel Loci for Non-Syndromic Coarctation of the Aorta in Sporadic and Familial Cases

BACKROUND: Coarctation of the aorta (CoA) accounts for 5-8% of all congenital heart defects. CoA can be detected in up to 20% of patients with Ullrich-Turner syndrome (UTS), in which a part or all of one of the X chromosomes is absent. The etiology of non-syndromic CoA is poorly understood. In the p...

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Detalles Bibliográficos
Autores principales: Moosmann, Julia, Uebe, Steffen, Dittrich, Sven, Rüffer, André, Ekici, Arif B., Toka, Okan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4436177/
https://www.ncbi.nlm.nih.gov/pubmed/25984793
http://dx.doi.org/10.1371/journal.pone.0126873

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4436177/
https://www.ncbi.nlm.nih.gov/pubmed/25984793
http://dx.doi.org/10.1371/journal.pone.0126873

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