Associations between common genetic variants in microRNAs and Hirschsprung disease susceptibility in Southern Chinese children

INTRODUCTION: Hirschsprung disease (HSCR), characterized by the defective migration of enteric neural crest cells, is a severe congenital tract disease in infants. Its etiology is not clear at present, although a genetic component plays an important role in its etiology. Many studies focused on the...

Πλήρης περιγραφή

Αποθηκεύτηκε σε:
Λεπτομέρειες βιβλιογραφικής εγγραφής
Τόπος έκδοσης:J Gene Med
Κύριοι συγγραφείς: Wu, Qi, Zhao, Jinglu, Zheng, Yi, Xie, Xiaoli, He, Qiuming, Zhu, Yun, Wang, Ning, Huang, Lihua, Lu, Lifeng, Hu, Tuqun, Zeng, Jixiao, Xia, Huimin, Zhang, Yan, Zhong, Wei
Μορφή: Artigo
Γλώσσα:Inglês
Έκδοση: John Wiley and Sons Inc. 2021
Θέματα:
Research Articles
Διαθέσιμο Online:https://ncbi.nlm.nih.gov/pmc/articles/PMC7900950/
https://ncbi.nlm.nih.gov/pubmed/33294994
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jgm.3301
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