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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Bibliographic Details
Published in:	J Transl Med
Main Authors:	Zhou, Shuang, Wang, Qingjie, Meng, Zhuo, Peng, Jiayu, Zhou, Yue, Song, Wenting, Wang, Jian, Chen, Sun, Sun, Kun
Format:	Artigo
Language:	Inglês
Published:	BioMed Central 2020
Subjects:	Research
Online Access:	https://ncbi.nlm.nih.gov/pmc/articles/PMC7362408/ https://ncbi.nlm.nih.gov/pubmed/32664970 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12967-020-02445-2
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Mutations in fibroblast growth factor (FGF8) and FGF10 identified in patients with conotruncal defects

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