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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Detalles Bibliográficos
Autores principales: Mengmeng, Xu, Yuejuan, Xu, Sun, Chen, Yanan, Lu, Fen, Li, Kun, Sun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7203814/
https://www.ncbi.nlm.nih.gov/pubmed/32380971
http://dx.doi.org/10.1186/s12881-020-01032-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7203814/
https://www.ncbi.nlm.nih.gov/pubmed/32380971
http://dx.doi.org/10.1186/s12881-020-01032-y

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