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Associations of SLC6A20 genetic polymorphisms with Hirschsprung’s disease in a Southern Chinese population
Hirschsprung’s disease (HSCR) is a neurodevelopmental disorder characterized by the absence of nerves in intestine with strong genetic components. SLC6A20 was found to be associated with HSCR in Korean population waiting for replication in an independent cohort. In the present study, ten single nucl...
में बचाया:
| में प्रकाशित: | Biosci Rep |
|---|---|
| मुख्य लेखकों: | , , , , , , , , |
| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
Portland Press Ltd.
2019
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| विषय: | |
| ऑनलाइन पहुंच: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6692567/ https://ncbi.nlm.nih.gov/pubmed/31358688 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1042/BSR20182290 |
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