Agxt-KO 基因敲除小鼠

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2. Boualla, Lamiae, Tajir, Mariam, Oulahiane, Najat, Ait Ouamar, Hassan, Sefiani, Abdelaziz. 2015. AGXT Gene Mutations and Prevalence of Primary Hyperoxaluria Type 1 in Moroccan Population. In Genetic testing and molecular biomarkers, 19, 623-8. doi:10.1089/gtmb.2015.0136. https://pubmed.ncbi.nlm.nih.gov/26383609/

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4. Ahmed, Hoda A, Fadel, Fatina I, Abdel Mawla, Mohamed A, Fathallah, Mohamed Gamal, Amr, Khalda. 2022. Next-generation sequencing in identification of pathogenic variants in primary hyperoxaluria among 21 Egyptian families: Identification of two novel AGXT gene mutations. In Molecular genetics & genomic medicine, 10, e1992. doi:10.1002/mgg3.1992. https://pubmed.ncbi.nlm.nih.gov/35661454/