1. Balakrishnan, Bijina, Altassan, Ruqaiah, Budhraja, Rohit, Morava, Eva, Lai, Kent. 2023. AAV-based gene therapy prevents and halts the progression of dilated cardiomyopathy in a mouse model of phosphoglucomutase 1 deficiency (PGM1-CDG). In Translational research : the journal of laboratory and clinical medicine, 257, 1-14. doi:10.1016/j.trsl.2023.01.004. https://pubmed.ncbi.nlm.nih.gov/36709920/
2. Tian, Wo-Tu, Luan, Xing-Hua, Zhou, Hai-Yan, Tang, Hui-Dong, Cao, Li. 2019. Congenital disorder of glycosylation type 1T with a novel truncated homozygous mutation in PGM1 gene and literature review. In Neuromuscular disorders : NMD, 29, 282-289. doi:10.1016/j.nmd.2019.01.001. https://pubmed.ncbi.nlm.nih.gov/30737079/
3. Zheng, Zhewen, Zhang, Xue, Bai, Jian, Liu, Di, Zhou, Yunfeng. 2022. PGM1 suppresses colorectal cancer cell migration and invasion by regulating the PI3K/AKT pathway. In Cancer cell international, 22, 201. doi:10.1186/s12935-022-02545-7. https://pubmed.ncbi.nlm.nih.gov/35614441/
4. Radenkovic, Silvia, Bleukx, Sofie, Engelhardt, Nicole, Edmondson, Andrew C, Morava, Eva. 2024. Coagulation abnormalities and vascular complications are common in PGM1-CDG. In Molecular genetics and metabolism, 142, 108530. doi:10.1016/j.ymgme.2024.108530. https://pubmed.ncbi.nlm.nih.gov/38968673/
5. Zhao, Wei, Cai, Zhengyun, Wei, Chuanhao, Gu, Yaling, Zhang, Juan. 2023. Functional identification of PGM1 in the regulating development and depositing of inosine monophosphate specific for myoblasts. In Frontiers in veterinary science, 10, 1276582. doi:10.3389/fvets.2023.1276582. https://pubmed.ncbi.nlm.nih.gov/38164393/