IGF2‐derived miR‐483‐3p associated with Hirschsprung's disease by targeting FHL1

HSCR (Hirschsprung's disease) is a serious congenital defect, and the aetiology of it remains unclear. Many studies have highlighted the significant roles of intronic miRNAs and their host genes in various disease, few was mentioned in HSCR although. In this study, miR‐483‐3p along with its hos...

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Detalles Bibliográficos
Autores principales: Zhi, Zhengke, Zhu, Hairong, Lv, Xiaofeng, Lu, Changgui, Li, Yang, Wu, Feng, Zhou, Lingling, Li, Hongxing, Tang, Weibing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6156468/
https://www.ncbi.nlm.nih.gov/pubmed/30073757
http://dx.doi.org/10.1111/jcmm.13756

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6156468/
https://www.ncbi.nlm.nih.gov/pubmed/30073757
http://dx.doi.org/10.1111/jcmm.13756

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