Magt1-KO 基因敲除小鼠

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3. Blommaert, Eline, Cherepanova, Natalia A, Staels, Frederik, Foulquier, François, Matthijs, Gert. 2022. Lack of NKG2D in MAGT1-deficient patients is caused by hypoglycosylation. In Human genetics, 141, 1279-1286. doi:10.1007/s00439-021-02400-1. https://pubmed.ncbi.nlm.nih.gov/35182234/

4. Kauskot, Alexandre, Mallebranche, Coralie, Bruneel, Arnaud, Miot, Charline, Adam, Frédéric. 2023. MAGT1 deficiency in XMEN disease is associated with severe platelet dysfunction and impaired platelet glycoprotein N-glycosylation. In Journal of thrombosis and haemostasis : JTH, 21, 3268-3278. doi:10.1016/j.jtha.2023.05.007. https://pubmed.ncbi.nlm.nih.gov/37207862/