MED20
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Mediator complex subunit 20 (Med20) is a protein that in humans is encoded by the MED20 gene.[1] Mutations in the MED20 are associated with basal ganglia degeneration and brain atrophy in infants.[2]
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References[edit]
- ^ Tang, Wen-Shuai; Weng, Li; Wang, Xu; Liu, Chang-Qin; Hu, Guo-Sheng; Yin, Shu-Ting; Tao, Ying; Hong, Ni-Na; Guo, Huiling; Liu, Wen; Wang, Hong-Rui; Zhao, Tong-Jin (July 2021). "The Mediator subunit MED20 organizes the early adipogenic complex to promote development of adipose tissues and diet-induced obesity". Cell Reports. 36 (1): 109314. doi:10.1016/j.celrep.2021.109314. ISSN 2211-1247.
- ^ Vodopiutz, Julia; Schmook, Maria T.; Konstantopoulou, Vassiliki; Plecko, Barbara; Greber-Platzer, Susanne; Creus, Marc; Seidl, Rainer; Janecke, Andreas R. (January 2015). "MED20 mutation associated with infantile basal ganglia degeneration and brain atrophy". European Journal of Pediatrics. 174 (1): 113–118. doi:10.1007/s00431-014-2463-7. ISSN 0340-6199.
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