De novo NFκB2 gene mutation associated common variable immunodeficiency
Objective: To investigate the clinical, immunological, and molecular manifestations of nuclear factor kappa-B subunit 2 (NFκB2) gene mutation associated common variable immunodeficiency (CVID) . Methods: A 14-month-old boy diagnosed with NFκB2-mutated CVID was admitted into Children's Hospital...
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Détails bibliographiques
| Publié dans: | Zhonghua er ke za zhi = Chinese journal of pediatrics. - 1960. - 56(2018), 8 vom: 02. Aug., Seite 628-632
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| Auteur principal: |
Luo, M Z
(Auteur) |
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| Autres auteurs: |
Xu, T,
Xue, X H,
Wang, Y P,
Wu, P L,
Chen, X M,
Tang, X M,
Zhao, X D,
Zhang, Z Y |
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| Format: | Article en ligne
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| Langue: | Chinese |
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| Publié: |
2018
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| Accès à la collection: | Zhonghua er ke za zhi = Chinese journal of pediatrics
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| Sujets: | Case Reports
Journal Article
Review
Adrenocorticotrophic hormone
Genes
Immunologic deficiency syndrome
NF-kappa B p52 Subunit
NFKB2 protein, human |
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