NFKB2 mutation in common variable immunodeficiency and isolated adrenocorticotropic hormone deficiency: A case report and review of literature
about
Novel nonsense gain-of-function NFKB2 mutations associated with a combined immunodeficiency phenotype.Human NF-κB1 Haploinsufficiency and Epstein-Barr Virus-Induced Disease-Molecular Mechanisms and Consequences.Bacille Calmette–Guerin Complications in Newly Described Primary Immunodeficiency Diseases: 2010–2017.
P2860
NFKB2 mutation in common variable immunodeficiency and isolated adrenocorticotropic hormone deficiency: A case report and review of literature
description
2016 nî lūn-bûn
@nan
2016 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2016 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
name
NFKB2 mutation in common varia ...... eport and review of literature
@ast
NFKB2 mutation in common varia ...... eport and review of literature
@en
NFKB2 mutation in common varia ...... eport and review of literature
@nl
type
label
NFKB2 mutation in common varia ...... eport and review of literature
@ast
NFKB2 mutation in common varia ...... eport and review of literature
@en
NFKB2 mutation in common varia ...... eport and review of literature
@nl
prefLabel
NFKB2 mutation in common varia ...... eport and review of literature
@ast
NFKB2 mutation in common varia ...... eport and review of literature
@en
NFKB2 mutation in common varia ...... eport and review of literature
@nl
P2093
P2860
P31
P921
P3181
P1433
P1476
NFKB2 mutation in common varia ...... eport and review of literature
@en
P2093
Hong-Mei Song
Wei-Bo Xia
Xiao-Qian Zhang
Yue-Hua Liu
Zheng-Yin Liu
P2860
P3181
P356
10.1097/MD.0000000000005081
P407
P5008
P577
2016-10-01T00:00:00Z