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Association of NRG1 and AUTS2 genetic polymorphisms with Hirschsprung disease in a South Chinese population
Hirschsprung disease (HSCR) is a genetic disorder characterized by the absence of enteric ganglia. There are more than 15 genes identified as contributed to HSCR by family‐based or population‐based approaches. However, these findings were not fulfilled to explain the heritability of most sporadic ca...
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| Publié dans: | J Cell Mol Med |
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| Auteurs principaux: | , , , , , , |
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
John Wiley and Sons Inc.
2018
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| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5867083/ https://ncbi.nlm.nih.gov/pubmed/29377512 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/jcmm.13498 |
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