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Novel mutations of the SRF gene in Chinese sporadic conotruncal heart defect patients
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 transcription fa...
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| Publicado no: | BMC Med Genet |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2020
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7203814/ https://ncbi.nlm.nih.gov/pubmed/32380971 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-020-01032-y |
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