Exome Analysis of a Family with Pleiotropic Congenital Heart Disease

BACKGROUND: A number of single gene defects have been identified in patients with isolated or nonsyndromic congenital heart defects (CHD). However, due to significant genetic heterogeneity candidate gene approaches have had limited success in finding high-risk alleles in most cases. OBJECTIVE: Use e...

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Bibliografski detalji
Glavni autori: Arrington, Cammon B., Bleyl, Steven B., Matsunami, Norisada, Bonnell, Gabriel D., Otterud, Brith E.M., Nielsen, Douglas C., Stevens, Jeffrey, Levy, Shawn, Leppert, Mark F., Bowles, Neil E.
Format: Artigo
Jezik:Inglês
Izdano: 2012
Teme:
Article
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3329568/
https://ncbi.nlm.nih.gov/pubmed/22337856
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/CIRCGENETICS.111.961797
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