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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...
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| Pubblicato in: | J Gene Med |
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| Autori principali: | , , , , , , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
John Wiley and Sons Inc.
2021
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| Soggetti: | |
| Accesso 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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