Pah-flox 基因敲除小鼠

1. Alibakhshi, Reza, Mohammadi, Aboozar, Salari, Nader, Kazeminia, Mohsen, Moradi, Keivan. 2021. Spectrum of PAH gene mutations in 1547 phenylketonuria patients from Iran: a comprehensive systematic review. In Metabolic brain disease, 36, 767-780. doi:10.1007/s11011-021-00698-4. https://pubmed.ncbi.nlm.nih.gov/33625639/

2. Yan, Yousheng, Zhang, Chuan, Jin, Xiaohua, Gao, Huafang, Ma, Xu. 2019. Mutation spectrum of PAH gene in phenylketonuria patients in Northwest China: identification of twenty novel variants. In Metabolic brain disease, 34, 733-745. doi:10.1007/s11011-019-0387-7. https://pubmed.ncbi.nlm.nih.gov/30747360/

3. Klaassen, Kristel, Stankovic, Biljana, Kotur, Nikola, Pavlovic, Sonja, Stojiljkovic, Maja. 2016. New PAH gene promoter KLF1 and 3'-region C/EBPalpha motifs influence transcription in vitro. In Journal of applied genetics, 58, 79-85. doi:10.1007/s13353-016-0359-0. https://pubmed.ncbi.nlm.nih.gov/27447460/

4. Razipour, Masoumeh, Alavinejad, Elaheh, Sajedi, Seyede Zahra, Mohaddes Ardebili, Seyyed Mojtaba, Keramatipour, Mohammad. 2017. Genetic study of the PAH locus in the Iranian population: familial gene mutations and minihaplotypes. In Metabolic brain disease, 32, 1685-1691. doi:10.1007/s11011-017-0048-7. https://pubmed.ncbi.nlm.nih.gov/28676969/