OMIA 001768-9986 : Non-specific digestive disorder in Oryctolagus cuniculus
Mendelian trait/disorder: unknown Considered a defect: yes History: Zhang et al. (2013) reported some associations between polymorphisms in the comparative candidate gene NOD2 and susceptibility to this disorder.
Note: the references are listed in reverse chronological order (from the most recent year to the earliest year), and alphabetically by first author within a year.
|2013||Chen, S.Y., Zhang, W.X., Zhang, G.W., Peng, J., Zhao, X.B., Lai, S.J. :|
|Case-control study and mRNA expression analysis reveal the MyD88 gene is associated with digestive disorders in rabbit. Anim Genet :, 2013. Pubmed reference: 23647105. DOI: 10.1111/age.12052.|
|Zhang, W.X., Zhang, G.W., Peng, J., Zhang, J.L., Yang, Y., Lai, S.J. :|
|A synonymous mutation in NOD2 gene was significantly associated with non-specific digestive disorder in rabbit. Gene 516:193-7, 2013. Pubmed reference: 23296055. DOI: 10.1016/j.gene.2012.12.091.|
- Created by Frank Nicholas on 18 Jan 2013