Mlycd-flox 基因敲除小鼠

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2. Zhang, J M, Hao, L L, Qiu, W J, Yang, S H, Han, L S. 2024. Clinical, biochemical and genetic characteristics and long-term follow-up of five patients with malonyl-CoA decarboxylase deficiency. In Brain & development, 46, 286-293. doi:10.1016/j.braindev.2024.07.001. https://pubmed.ncbi.nlm.nih.gov/39069445/

3. Xu, Fang, Wu, Yangyang, Huang, Jiyi, Duan, Junkai, Li, Hong. 2023. Case report: A novel 5'-UTR-exon1-intron1 deletion in MLYCD in an IVF child with malonyl coenzyme A decarboxylase deficiency and literature review. In Frontiers in medicine, 10, 1160879. doi:10.3389/fmed.2023.1160879. https://pubmed.ncbi.nlm.nih.gov/37206471/