The interplay of common genetic variants NRG1 rs2439302 and RET rs2435357 increases the risk of developing Hirschsprung’s disease

Introduction: As a congenital and genetically related disease, many single nucleotide polymorphisms (SNPs) have been reported to be associated with the risk of HSCR. Our previous research showed that SNP rs2439302 (NRG1) interacted with rs2435357 (RET) to increase the risk of HSCR development. Howev...

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Detalles Bibliográficos
Autores principales: Chi, Shuiqing, Li, Shuai, Cao, Guoqing, Guo, Jialing, Han, Yunqiao, Zhou, Yun, Zhang, Xi, Li, Yibo, Luo, Zhibin, Li, Xiangyang, Rong, Liying, Zhang, Mengxin, Li, Linglu, Tang, Shaotao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Cell and Developmental Biology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10361661/
https://www.ncbi.nlm.nih.gov/pubmed/37484916
http://dx.doi.org/10.3389/fcell.2023.1184799

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10361661/
https://www.ncbi.nlm.nih.gov/pubmed/37484916
http://dx.doi.org/10.3389/fcell.2023.1184799

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