Φορτώνει......
Identification of Functional Mutations in GATA4 in Patients with Congenital Heart Disease
Congenital heart disease (CHD) is one of the most prevalent developmental anomalies and the leading cause of noninfectious morbidity and mortality in newborns. Despite its prevalence and clinical significance, the etiology of CHD remains largely unknown. GATA4 is a highly conserved transcription fac...
Αποθηκεύτηκε σε:
| Κύριοι συγγραφείς: | , , , , , , , , , , , |
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| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Public Library of Science
2013
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3633926/ https://ncbi.nlm.nih.gov/pubmed/23626780 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0062138 |
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