Rare mendelian primary immunodeficiency diseases associated with impaired NF-κB signaling
about
NFKB2 mutation in common variable immunodeficiency and isolated adrenocorticotropic hormone deficiency: A case report and review of literatureCognitive-behavioural phenotype in a group of girls from 1.2 to 12 years old with the Incontinentia Pigmenti syndrome: Recommendations for clinical management.Bacille Calmette–Guerin Complications in Newly Described Primary Immunodeficiency Diseases: 2010–2017.
P2860
Rare mendelian primary immunodeficiency diseases associated with impaired NF-κB signaling
description
2015 nî lūn-bûn
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2015年の論文
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2015年学术文章
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2015年学术文章
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2015年学术文章
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2015年学术文章
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2015年学术文章
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2015年學術文章
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2015年學術文章
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2015年學術文章
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name
Rare mendelian primary immunodeficiency diseases associated with impaired NF-κB signaling
@en
type
label
Rare mendelian primary immunodeficiency diseases associated with impaired NF-κB signaling
@en
prefLabel
Rare mendelian primary immunodeficiency diseases associated with impaired NF-κB signaling
@en
P2093
P2860
P921
P356
P1433
P1476
Rare mendelian primary immunodeficiency diseases associated with impaired NF-κB signaling
@en
P2093
A Pescatore
E Esposito
M Paciolla
M V Ursini
P2860
P2888
P304
P356
10.1038/GENE.2015.3
P577
2015-03-12T00:00:00Z
2015-06-01T00:00:00Z
P5875
P6179
1013653636