1. Barc, Julien, Tadros, Rafik, Glinge, Charlotte, Redon, Richard, Bezzina, Connie R. 2022. Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility. In Nature genetics, 54, 232-239. doi:10.1038/s41588-021-01007-6. https://pubmed.ncbi.nlm.nih.gov/35210625/
2. Gowda, Vykuntaraju K, Srinivasan, Varunvenkat M, Reddy, Varsha, Bhat, Maya. 2021. Rare Cause of West syndrome secondary to Tubulinopathy due to Congenital Symmetric Circumferential Skin Creases (CSCSC) Kunze Type due to a Novel Variant in MAPRE2 Gene. In Annals of Indian Academy of Neurology, 25, 283-285. doi:10.4103/aian.AIAN_420_21. https://pubmed.ncbi.nlm.nih.gov/35693690/
3. Peng, Lu, Li, Nianshen, Huang, Zhanrong, Qiu, Chunqin, Yin, Shihua. 2022. Prognostic Gene Expression Signature for Age-Related Hearing Loss. In Frontiers in medicine, 9, 814851. doi:10.3389/fmed.2022.814851. https://pubmed.ncbi.nlm.nih.gov/35463035/
4. Isrie, Mala, Breuss, Martin, Tian, Guoling, Keays, David Anthony, Van Esch, Hilde. . Mutations in Either TUBB or MAPRE2 Cause Circumferential Skin Creases Kunze Type. In American journal of human genetics, 97, 790-800. doi:10.1016/j.ajhg.2015.10.014. https://pubmed.ncbi.nlm.nih.gov/26637975/
5. Zhang, Deming, Pan, Gaofeng, Cheng, Nitao, Li, Changsheng, Zhao, Jinping. 2022. JUND facilitates proliferation and angiogenesis of esophageal squamous cell carcinoma cell via MAPRE2 up-regulation. In Tissue & cell, 81, 102010. doi:10.1016/j.tice.2022.102010. https://pubmed.ncbi.nlm.nih.gov/36608637/
智鼠故事 
