TPM3 deletions cause a hypercontractile congenital muscle stiffness phenotype
TPM3基因缺失会导致先天性肌肉过度收缩僵硬表型
期刊:Annals of Neurology
影响因子:7.7
doi:10.1002/ana.24535
Donkervoort, S; Papadaki, M; de Winter, J M; Neu, M B; Kirschner, J; Bolduc, V; Yang, M L; Gibbons, M A; Hu, Y; Dastgir, J; Leach, M E; Rutkowski, A; Foley, A R; Krüger, M; Wartchow, E P; McNamara, E; Ong, R; Nowak, K J; Laing, N G; Clarke, N F; Ottenheijm, Cac; Marston, S B; Bönnemann, C G