Novel mutations of the SRF gene in Chinese sporadic conotruncal heart defect patients
Abstract Background Conotruncal heart defects (CTDs) are a group of congenital heart malformations that cause anomalies of cardiac outflow tracts. In the past few decades, many genes related to CTDs have been reported. Serum response factor (SRF) is a ubiquitous nuclear protein that acts as transcri...
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| Автори: | , , , , , |
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| Формат: | Artigo |
| Мова: | Inglês |
| Опубліковано: |
BMC
2020-05-01
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| Серія: | BMC Medical Genetics |
| Предмети: | |
| Онлайн доступ: | http://link.springer.com/article/10.1186/s12881-020-01032-y |
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