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Two Heterozygous Mutations in NFATC1 in a Patient with Tricuspid Atresia
Tricuspid Atresia (TA) is a rare form of congenital heart disease (CHD) with usually poor prognosis in humans. It presents as a complete absence of the right atrio-ventricular connection secured normally by the tricuspid valve. Defects in the tricuspid valve are so far not associated with any geneti...
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Main Authors: | , , , , , , , , , |
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Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
Public Library of Science
2012
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Assuntos: | |
Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3511479/ https://ncbi.nlm.nih.gov/pubmed/23226213 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0049532 |
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