1. Hammill, Adrienne M, Boscolo, Elisa. 2024. Capillary malformations. In The Journal of clinical investigation, 134, . doi:10.1172/JCI172842. https://pubmed.ncbi.nlm.nih.gov/38618955/
2. Sánchez-Espino, Luis Fernando, Ivars, Marta, Antoñanzas, Javier, Baselga, Eulalia. 2023. Sturge-Weber Syndrome: A Review of Pathophysiology, Genetics, Clinical Features, and Current Management Approache. In The application of clinical genetics, 16, 63-81. doi:10.2147/TACG.S363685. https://pubmed.ncbi.nlm.nih.gov/37124240/
3. Li, Dandan, Ling, Xi, Li, Xiaoqing, Li, Xingang, Ma, Ning. 2022. Association between GNAQ Gene DNA Methylation and Vascular Recurrence in Patients with Acute Ischemic Stroke or Transient Ischemic Attack. In Cerebrovascular diseases (Basel, Switzerland), 51, 712-721. doi:10.1159/000524416. https://pubmed.ncbi.nlm.nih.gov/35764070/
4. Feng, Xiaodong, Arang, Nadia, Rigiracciolo, Damiano Cosimo, Ruppin, Eytan, Gutkind, J Silvio. 2019. A Platform of Synthetic Lethal Gene Interaction Networks Reveals that the GNAQ Uveal Melanoma Oncogene Controls the Hippo Pathway through FAK. In Cancer cell, 35, 457-472.e5. doi:10.1016/j.ccell.2019.01.009. https://pubmed.ncbi.nlm.nih.gov/30773340/
5. Liau, Jau-Yu, Tsai, Jia-Huei, Lan, Jui, Lee, Jen-Chieh, Huang, Hsuan-Ying. 2019. GNA11 joins GNAQ and GNA14 as a recurrently mutated gene in anastomosing hemangioma. In Virchows Archiv : an international journal of pathology, 476, 475-481. doi:10.1007/s00428-019-02673-y. https://pubmed.ncbi.nlm.nih.gov/31707589/
智鼠故事 
