Lv31
232 积分 2024-06-03 加入
Review of the Pathophysiology and Clinical Manifestations of 22q11.2 Deletion and Duplication Syndromes
4小时前
已完结
Cognitive and behaviour profiles of children with mucopolysaccharidosis Type II
20天前
已完结
The pathogenesis of gout: molecular insights from genetic, epigenomic and transcriptomic studies
20天前
已完结
Characterization of a HIR-Fab-IDS, Novel Iduronate 2-Sulfatase Fusion Protein for the Treatment of Neuropathic Mucopolysaccharidosis Type II (Hunter Syndrome)
26天前
已完结
Genetics and Gene Therapy in Hunter Disease
28天前
已关闭
Analytical validation of the amplification refractory mutation system polymerase chain reaction-capillary electrophoresis assay to diagnose spinal muscular atrophy
1个月前
已完结
Processing of iduronate 2-sulphatase in human fibroblasts
1个月前
已完结
Hurler and Hunter Syndromes: Mutual Correction of the Defect in Cultured Fibroblasts
1个月前
已完结
Development of idursulfase therapy for mucopolysaccharidosis type II (Hunter syndrome): the past, the present and the future
1个月前
已完结
Iduronate-2-sulfatase transport vehicle rescues behavioral and skeletal phenotypes in a mouse model of Hunter syndrome
1个月前
已完结
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