Mutations in fibroblast growth factor (FGF8) and FGF10 identified in patients with conotruncal defects

BACKGROUND: Conotruncal defects (CTDs) are a type of heterogeneous congenital heart diseases (CHDs), but little is known about their etiology. Increasing evidence has demonstrated that fibroblast growth factor (FGF) 8 and FGF10 may be involved in the pathogenesis of CTDs. METHODS: The variants of FG...

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Detalles Bibliográficos
Autores principales: Zhou, Shuang, Wang, Qingjie, Meng, Zhuo, Peng, Jiayu, Zhou, Yue, Song, Wenting, Wang, Jian, Chen, Sun, Sun, Kun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7362408/
https://www.ncbi.nlm.nih.gov/pubmed/32664970
http://dx.doi.org/10.1186/s12967-020-02445-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7362408/
https://www.ncbi.nlm.nih.gov/pubmed/32664970
http://dx.doi.org/10.1186/s12967-020-02445-2

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