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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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Bibliografiske detaljer
Udgivet i:J Cell Mol Med
Main Authors: Zhi, Zhengke, Zhu, Hairong, Lv, Xiaofeng, Lu, Changgui, Li, Yang, Wu, Feng, Zhou, Lingling, Li, Hongxing, Tang, Weibing
Format: Artigo
Sprog:Inglês
Udgivet: John Wiley and Sons Inc. 2018
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6156468/
https://ncbi.nlm.nih.gov/pubmed/30073757
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/jcmm.13756
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