Structural and functional analysis of perforin mutations in association with clinical data of familial hemophagocytic lymphohistiocytosis type 2 (FHL2) patients

• المؤلفون الرئيسيون: An, O, Gursoy, A, Gurgey, A, Keskin, O
• مؤلفون آخرون: CANCER SCIENCE INSTITUTE OF SINGAPORE
• التنسيق: مقال
• منشور في: Wiley 2019
• الموضوعات: Adolescent; Adult; Child; Child, Preschool; Female; Humans; Infant; Infant, Newborn; Lymphohistiocytosis, Hemophagocytic; Male; Models, Molecular; Mutation, Missense; Perforin; Polymorphism, Single Nucleotide; Protein Conformation; Young Adult
• الوصول للمادة أونلاين: https://scholarbank.nus.edu.sg/handle/10635/155280

10.1002/pro.2265