Patient reported outcomes for phosphomannomutase 2 congenital disorder of glycosylation (PMM2-CDG): listening to what matters for the patients and health professionals
磷酸甘露糖变位酶 2 先天性糖基化障碍 (PMM2-CDG) 的患者报告结局:倾听患者和医护人员的心声
期刊:Orphanet Journal of Rare Diseases
影响因子:3.5
doi:10.1186/s13023-022-02551-y
Pascoal, C; Ferreira, I; Teixeira, C; Almeida, E; Slade, A; Brasil, S; Francisco, R; Ligezka, A N; Morava, E; Plotkin, H; Jaeken, J; Videira, P A; Barros, L; Dos Reis Ferreira, V