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American Journal of Medical Genetics|March 2, 1999
Screen for MAOA mutations in target human groupsD E Schuback, E L Mulligan, K B Sims, et al.Human Molecular Genetics|January 9, 2013
Cathepsin F mutations cause Type B Kufs disease, an adult-onset neuronal ceroid lipofuscinosisKatherine R Smith, Hans-Henrik M Dahl, Laura Canafoglia, et al.Human Molecular Genetics|November 26, 2013
Human iPSC models of neuronal ceroid lipofuscinosis capture distinct effects of TPP1 and CLN3 mutations on the endocytic pathwayXenia Lojewski, John F Staropoli, Sunita Biswas-Legrand, et al.Science (New York, N.Y.)|February 21, 2015
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathwaysElizabeth T Cirulli, Brittany N Lasseigne, Slavé Petrovski, et al.Proceedings of the National Academy of Sciences of the United States of America|February 15, 2022
Pharmaceutical pollution of the world's riversJohn L Wilkinson, Alistair B A Boxall, Dana W Kolpin, et al.Pageof 20