학술논문
Mutations in the selenocysteine insertion sequence-binding protein 2 gene lead to a multisystem selenoprotein deficiency disorder in humans
Document Type
Article
Author
Schoenmakers, E.; Agostini, M.; Mitchell, C.; Schoenmakers, N.; Rajanayagam, O.; Castanet, M.; Groeneveld, M.; Campi, I.; Blount, M.; Burton, H.; Semple, R.; Gurnell, M.; Chatterjee, V.K.K.; Papp, L.; Khanna, K.K.; Padidela, R.; Dattani, M.; Ceron-Gutierrez, L.; Doffinger, R.; Prevosto, C.; Gaston, H.; Luan, J.; Wareham, N.; Montano, S.; Lu, J.; Holmgren, A.; Clemons, N.; Fitzgerald, R.; Castets, P.; Guicheney, P.; Karbaschi, M.; Cooke, M.; Aitken, S.; Dixon, A.; Williams, J.; Muntoni, F.; O'Donovan, D.; Dean, A.; Warren, A.; Brierley, C.; Baguley, D.; Coles, A.; Todd, P.; Halsall, D.; Schwabe, J.; Grasso, L.; Beck-Peccoz, P.; Ogunko, A.
Source
In: Journal of Clinical Investigation . (Journal of Clinical Investigation, 1 December 2010, 120(12):4220-4235)
Subject
Language
English
ISSN
00219738
15588238
15588238