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AB097. Combined effects of RET transcriptional enhancer 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 was identified as a major locus involved in HSCR. In this study, we investigated the joint effects of common vari...
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| Publicado en: | Ann Transl Med |
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| Autores principales: | , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
AME Publishing Company
2017
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5641765/ https://ncbi.nlm.nih.govhttp://dx.doi.org/10.21037/atm.2017.s097 |
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