Information Journal Paper
APA:
Copy. (2019). Novel Heterozygous Mutation in NFKB2 Is Associated With Early Onset CVID and a Functional Defect in NK Cells Complicated by Disseminated CMV Infection and Severe Nephrotic Syndrome. Frontiers in pediatrics, 7(-), 0-0. SID. https://sid.ir/paper/761775/en
Vancouver:
Copy. Novel Heterozygous Mutation in NFKB2 Is Associated With Early Onset CVID and a Functional Defect in NK Cells Complicated by Disseminated CMV Infection and Severe Nephrotic Syndrome. Frontiers in pediatrics[Internet]. 2019;7(-):0-0. Available from: https://sid.ir/paper/761775/en
IEEE:
Copy, “Novel Heterozygous Mutation in NFKB2 Is Associated With Early Onset CVID and a Functional Defect in NK Cells Complicated by Disseminated CMV Infection and Severe Nephrotic Syndrome,” Frontiers in pediatrics, vol. 7, no. -, pp. 0–0, 2019, [Online]. Available: https://sid.ir/paper/761775/en