학술논문
Mutations in the selenocysteine insertion sequence-binding protein 2 gene lead to a multisystem selenoprotein deficiency disorder in humans
Document Type
Artikel
Author
Schoenmakers, E; Agostini, M; Mitchell, C; Schoenmakers, N; Papp, L; Rajanayagam, O; Padidela, R; Ceron-Gutierrez, L; Doffinger, R; Prevosto, C; Luan, J; Montano, S; Lu, J; Castanet, M; Clemons, N; Groeneveld, M; Castets, P; Karbaschi, M; Aitken, S; Dixon, A; Williams, J; Campi, I; Blount, M; Burton, H; Muntoni, F; O'Donovan, D; Dean, A; Warren, A; Brierley, C; Baguley, D; Guicheney, P; Fitzgerald, R; Coles, A; Gaston, H; Todd, P; Holmgren, A; Khanna, KK; Cooke, M; Semple, R; Halsall, D; Wareham, N; Schwabe, J; Grasso, L; Beck-Peccoz, P; Ogunko, A; Dattani, M; Gurnell, M; Chatterjee, K
Source
The Journal of clinical investigation. 120(12):4220-4235
Subject
Language
English
English
English
ISSN
1558-8238