Coq7-flox 基因敲除小鼠

1. Jacquier, Arnaud, Theuriet, Julian, Fontaine, Fanny, Pegat, Antoine, Schaeffer, Laurent. . Homozygous COQ7 mutation: a new cause of potentially treatable distal hereditary motor neuropathy. In Brain : a journal of neurology, 146, 3470-3483. doi:10.1093/brain/awac453. https://pubmed.ncbi.nlm.nih.gov/36454683/

2. Qiu, Yusen, Xiong, Ying, Wang, Lulu, Tan, Dandan, Hong, Daojun. 2024. Homozygous variant in COQ7 causes autosomal recessive hereditary spastic paraplegia. In Annals of clinical and translational neurology, 11, 1067-1074. doi:10.1002/acn3.52037. https://pubmed.ncbi.nlm.nih.gov/38439593/

3. Marbois, B N, Clarke, C F. . The COQ7 gene encodes a protein in saccharomyces cerevisiae necessary for ubiquinone biosynthesis. In The Journal of biological chemistry, 271, 2995-3004. doi:. https://pubmed.ncbi.nlm.nih.gov/8621692/

4. Jonassen, T, Marbois, B N, Kim, L, Lusis, A J, Clarke, C F. . Isolation and sequencing of the rat Coq7 gene and the mapping of mouse Coq7 to chromosome 7. In Archives of biochemistry and biophysics, 330, 285-9. doi:. https://pubmed.ncbi.nlm.nih.gov/8660658/