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A Novel Missense Mutation of GATA4 in a Chinese Family with Congenital Heart Disease
BACKGROUND: Congenital heart disease (CHD) is the most prevalent type of birth defect in human, with high morbidity in infant. Several genes essential for heart development have been identified. GATA4 is a pivotal transcription factor that can regulate the cardiac development. Many GATA4 mutations h...
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| Publicado no: | PLoS One |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Public Library of Science
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4938561/ https://ncbi.nlm.nih.gov/pubmed/27391137 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0158904 |
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