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AB087. Synergistic genetic effects of RET and NRG1 susceptibility variants in Hirschsprung disease
BACKGROUND: Hirschsprung disease (HSCR) is a complex genetic disorder, which characterized by absence of ganglion cells along variable lengths of the intestines in neonates, with the RET and NRG1 are reported as the most common susceptible genes for HSCR development. Here, we investigated three comm...
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| Publicado no: | Ann Transl Med |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
AME Publishing Company
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5641813/ https://ncbi.nlm.nih.govhttp://dx.doi.org/10.21037/atm.2017.s087 |
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