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Significance of neurexin and neuroligin polymorphisms in regulating risk of Hirschsprung’s disease
By performing a basic case–control study among a Chinese population, the aims of this study were to explore if single nucleotide polymorphisms (SNPs) within neurexin and neuroligin were associated with susceptibility to Hirschsprung’s disease (HD). Eleven SNPs within neurexin and neuroligin were sel...
| Autores principales: | , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
BMJ Publishing Group
2018
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5992363/ https://www.ncbi.nlm.nih.gov/pubmed/29622757 http://dx.doi.org/10.1136/jim-2017-000623 |