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Rauch, F.; Moffatt, P.; Cheung, M.; Roughley, P.; Lalic, L.; Lund, A. M.; Ramirez, N.; Fahiminiya, S.; Majewski, J.; Glorieux, F. H. . (2013). Osteogenesis imperfecta type V: marked phenotypic variability despite the presence of the IFITM5 c.-14C>T mutation in all patients. Journal of Medical Genetics, 50(1), 21–24. doi:10.1136/jmedgenet-2012-101307 
An interview with Sci-Hub Founder Alexandra Elbakyan,Who exactly should pay for academic research