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miR-100 rs1834306 A>G Increases the Risk of Hirschsprung Disease in Southern Chinese Children
BACKGROUND: Hirschsprung disease (HSCR) is a rare congenital gastrointestinal disease characterized by the absence of intestinal submucosal and myometrial ganglion cells. Recently, researches indicated that miR-100 regulated the growth, differentiation and apoptosis of neurons, and affected the func...
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| Pubblicato in: | Pharmgenomics Pers Med |
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| Autori principali: | , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Dove
2020
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7428404/ https://ncbi.nlm.nih.gov/pubmed/32848443 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/PGPM.S265730 |
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