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Identification of GATA6 sequence variants in patients with congenital heart defects
While the etiology for the majority of congenital heart disease (CHD) remains poorly understood, the known genetic causes are often the result of mutations in cardiac developmental genes. GATA6 encodes for a cardiac transcription factor, which is broadly expressed in the developing heart and is crit...
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| Autori principali: | , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2010
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2940936/ https://ncbi.nlm.nih.gov/pubmed/20581743 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1203/PDR.0b013e3181ed17e4 |
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