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.
- DOI
- 10.3389/fped.2019.00303
- Published
- 2019
- Container
- Frontiers in pediatrics
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.3389/fped.2019.00303,
title = {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.},
author = {Aird A and Lagos M and Vargas-Hernández A and Posey JE and Coban-Akdemir Z and Jhangiani S and Mace EM and Reyes A and King A and Cavagnaro F and Forbes LR and Chinn IK and Lupski JR and Orange JS and Poli MC},
year = {2019},
journal = {Frontiers in pediatrics},
doi = {10.3389/fped.2019.00303},
url = {https://doi.org/10.3389/fped.2019.00303}
}RIS
TY - JOUR TI - 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. AU - Aird A AU - Lagos M AU - Vargas-Hernández A AU - Posey JE AU - Coban-Akdemir Z AU - Jhangiani S AU - Mace EM AU - Reyes A AU - King A AU - Cavagnaro F AU - Forbes LR AU - Chinn IK AU - Lupski JR AU - Orange JS AU - Poli MC PY - 2019 JO - Frontiers in pediatrics DO - 10.3389/fped.2019.00303 UR - https://doi.org/10.3389/fped.2019.00303 ER -
APA
A, A., M, L., A, V., JE, P., Z, C., S, J., EM, M., A, R., A, K., F, C., LR, F., IK, C., JR, L., JS, O., & MC, P. (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. https://doi.org/10.3389/fped.2019.00303
Source records
- pubmed · retrieved 2026-09-26T14:46:44.533Z