1. Chen, Qian, Zheng, Wen, Xu, Hongbo, Yuan, Lamei, Deng, Hao. 2021. Digenic Variants in the TTN and TRAPPC11 Genes Co-segregating With a Limb-Girdle Muscular Dystrophy in a Han Chinese Family. In Frontiers in neuroscience, 15, 601757. doi:10.3389/fnins.2021.601757. https://pubmed.ncbi.nlm.nih.gov/33746696/
2. Larson, Austin A, Baker, Peter R, Milev, Miroslav P, Sacher, Michael, Moore, Steven A. 2018. TRAPPC11 and GOSR2 mutations associate with hypoglycosylation of α-dystroglycan and muscular dystrophy. In Skeletal muscle, 8, 17. doi:10.1186/s13395-018-0163-0. https://pubmed.ncbi.nlm.nih.gov/29855340/
3. Matalonga, Leslie, Bravo, Miren, Serra-Peinado, Carla, Tort, Frederic, Girós, Marisa. 2016. Mutations in TRAPPC11 are associated with a congenital disorder of glycosylation. In Human mutation, 38, 148-151. doi:10.1002/humu.23145. https://pubmed.ncbi.nlm.nih.gov/27862579/
4. Wang, Xike, Wu, Yue, Cui, Yuxia, Folkersen, Lasse, Wang, Yuchuan. 2018. Novel TRAPPC11 Mutations in a Chinese Pedigree of Limb Girdle Muscular Dystrophy. In Case reports in genetics, 2018, 8090797. doi:10.1155/2018/8090797. https://pubmed.ncbi.nlm.nih.gov/30105108/
5. Koehler, Katrin, Milev, Miroslav P, Prematilake, Keshika, Huebner, Angela, Sacher, Michael. 2016. A novel TRAPPC11 mutation in two Turkish families associated with cerebral atrophy, global retardation, scoliosis, achalasia and alacrima. In Journal of medical genetics, 54, 176-185. doi:10.1136/jmedgenet-2016-104108. https://pubmed.ncbi.nlm.nih.gov/27707803/
智鼠故事 
