Dcdc2b-KO 基因敲除小鼠

1. Bieder, Andrea, Chandrasekar, Gayathri, Wason, Arpit, Kere, Juha, Tapia-Páez, Isabel. 2023. Genetic and protein interaction studies between the ciliary dyslexia candidate genes DYX1C1 and DCDC2. In BMC molecular and cell biology, 24, 20. doi:10.1186/s12860-023-00483-4. https://pubmed.ncbi.nlm.nih.gov/37237337/

2. Grati, M'hamed, Chakchouk, Imen, Ma, Qi, Liu, Xue Zhong, Masmoudi, Saber. 2015. A missense mutation in DCDC2 causes human recessive deafness DFNB66, likely by interfering with sensory hair cell and supporting cell cilia length regulation. In Human molecular genetics, 24, 2482-91. doi:10.1093/hmg/ddv009. https://pubmed.ncbi.nlm.nih.gov/25601850/