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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...
Tallennettuna:
| Julkaisussa: | PLoS One |
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| Päätekijät: | , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Public Library of Science
2015
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4436177/ https://ncbi.nlm.nih.gov/pubmed/25984793 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0126873 |
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