Or8b4-flox 基因敲除小鼠

1. Cheng, Shiqiang, Cheng, Bolun, Liu, Li, Jia, Yumeng, Zhang, Feng. 2022. Exome-wide screening identifies novel rare risk variants for major depression disorder. In Molecular psychiatry, 27, 3069-3074. doi:10.1038/s41380-022-01536-4. https://pubmed.ncbi.nlm.nih.gov/35365804/

2. Kajii, Takashi S, Oka, Akira, Saito, Fumio, Mitsui, Jun, Iida, Junichiro. 2019. Whole-exome sequencing in a Japanese pedigree implicates a rare non-synonymous single-nucleotide variant in BEST3 as a candidate for mandibular prognathism. In Bone, 122, 193-198. doi:10.1016/j.bone.2019.03.004. https://pubmed.ncbi.nlm.nih.gov/30849546/