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Novel GATA6 Mutations Associated with Congenital Ventricular Septal Defect or Tetralogy of Fallot
Congenital heart disease (CHD) is the most common form of developmental malformation and is the leading noninfectious cause of infant mortality. Emerging evidence indicates that genetic defects are involved in the pathogenesis of CHD. Nevertheless, CHD is genetically heterogeneous, and the molecular...
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| Main Authors: | , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Mary Ann Liebert, Inc.
2012
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3482375/ https://ncbi.nlm.nih.gov/pubmed/23020118 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1089/dna.2012.1814 |
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