Nfix-flox 基因敲除小鼠

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3. Jezela-Stanek, Aleksandra, Kucharczyk, Marzena, Falana, Katarzyna, Ploski, Rafal, Krajewska-Walasek, Malgorzata. 2016. Malan syndrome (Sotos syndrome 2) in two patients with 19p13.2 deletion encompassing NFIX gene and novel NFIX sequence variant. In Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia, 160, 161-7. doi:10.5507/bp.2016.006. https://pubmed.ncbi.nlm.nih.gov/26927468/