The analysis of DMD gene deletions by multiplex PCR in Indonesian DMD/BMD patients: The era of personalized medicine

• المؤلفون الرئيسيون: Iskandar, K, Dwianingsih, EK, Pratiwi, L, Kalim, AS, Mardhiah, H, Putranti, AH, Nurputra, DK, Triono, A, Herini, ES, Malueka, RG, Gunadi, Lai, PS, Sunartini
• مؤلفون آخرون: DUKE-NUS MEDICAL SCHOOL
• التنسيق: مقال
• منشور في: Springer Science and Business Media LLC 2021
• الموضوعات: DMD gene deletion; Duchenne/Becker muscular dystrophy; Exon skipping therapy; Multiplex PCR; Adolescent; Child; Child, Preschool; Dystrophin; Exons; Gene Deletion; Humans; Indonesia; Infant; Male; Multiplex Polymerase Chain Reaction; Muscular Dystrophy, Duchenne; Precision Medicine
• الوصول للمادة أونلاين: https://scholarbank.nus.edu.sg/handle/10635/206168

10.1186/s13104-019-4730-1