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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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| Gepubliceerd in: | J Transl Med |
|---|---|
| Hoofdauteurs: | , , , , , , , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
BioMed Central
2020
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| Onderwerpen: | |
| Online toegang: | 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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