1. Ye, Wen, Chen, Ao, Xu, Lingna, Sun, Dongxiao, Han, Bo. 2024. Single nucleotide polymorphisms of GYS2 gene and its association with milk production traits of dairy cows. In Animal biotechnology, 35, 2432966. doi:10.1080/10495398.2024.2432966. https://pubmed.ncbi.nlm.nih.gov/39629739/
2. Nessa, Azizun, Kumaran, Anitha, Kirk, Richard, Ismail, Dunia, Hussain, Khalid. . Mutational analysis of the GYS2 gene in patients diagnosed with ketotic hypoglycaemia. In Journal of pediatric endocrinology & metabolism : JPEM, 25, 963-7. doi:10.1515/jpem-2012-0165. https://pubmed.ncbi.nlm.nih.gov/23426827/
3. Chen, Shi-Lu, Zhang, Chris Zhiyi, Liu, Li-Li, Xie, Dan, Yun, Jing-Ping. 2018. A GYS2/p53 Negative Feedback Loop Restricts Tumor Growth in HBV-Related Hepatocellular Carcinoma. In Cancer research, 79, 534-545. doi:10.1158/0008-5472.CAN-18-2357. https://pubmed.ncbi.nlm.nih.gov/30584071/
4. Kamenets, Elena A, Gusarova, Elena A, Milovanova, Natalia V, Nikitina, Natalia V, Zakharova, Ekaterina Y. 2020. Hepatic glycogen synthase (GYS2) deficiency: seven novel patients and seven novel variants. In JIMD reports, 53, 39-44. doi:10.1002/jmd2.12082. https://pubmed.ncbi.nlm.nih.gov/32395408/
5. Arko, Janez Jan, Debeljak, Marusa, Tansek, Mojca Zerjav, Battelino, Tadej, Groselj, Urh. . A patient with glycogen storage disease type 0 and a novel sequence variant in GYS2: a case report and literature review. In The Journal of international medical research, 48, 300060520936857. doi:10.1177/0300060520936857. https://pubmed.ncbi.nlm.nih.gov/32779500/
6. Liao, Yinting, Tian, Yang, Li, Xiaojing, Liang, Huici, Chen, Wenxiong. . [Glycogen storage syndrome type 0 caused by GYS2 gene variation and phenotypic differences between two siblings]. In Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics, 38, 1110-1113. doi:10.3760/cma.j.cn511374-20200511-00336. https://pubmed.ncbi.nlm.nih.gov/34729754/
7. Ilyas, Muhammad, Holzwarth, Dorothea, Ishaq, Rafaqat, Kunz, Wolfram S, Shaiq, Pakeeza Arzoo. 2023. Whole-Exome sequencing identifies GYS2 biallelic variants in individuals with suspected epilepsy. In Seizure, 116, 74-80. doi:10.1016/j.seizure.2023.07.020. https://pubmed.ncbi.nlm.nih.gov/37574425/
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