Omenn syndrome associated with a functional reversion due to a somatic second-site mutation in CARD11 deficiency.
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Primary immunodeficiencies associated with eosinophiliaAutoimmunity in primary T-cell immunodeficiencies.Germline mutations predisposing to diffuse large B-cell lymphoma.30 Years of NF-κB: A Blossoming of Relevance to Human Pathobiology.Germline hypomorphic CARD11 mutations in severe atopic disease.Bacille Calmette–Guerin Complications in Newly Described Primary Immunodeficiency Diseases: 2010–2017.The CBM-opathies-A Rapidly Expanding Spectrum of Human Inborn Errors of Immunity Caused by Mutations in the CARD11-BCL10-MALT1 Complex
P2860
Q26746046-5ED02ABF-0B34-41B7-8905-50F5CE5F6C2FQ30251616-29E16D5B-C096-46B5-B8E8-D9C0E1B21217Q38756189-E2CE5A56-8003-4989-8A7E-C23396E2AE63Q39086011-9513173E-1516-484E-94E1-0EE0116ECC21Q39142799-BECCE089-70FD-4FE1-9225-67FA4BAA1152Q55514852-B029B625-AB6D-4D05-96EC-E6A13C1F2844Q57072726-44EB8E31-7BF5-4CCC-8EBB-F17EB14B7C20
P2860
Omenn syndrome associated with a functional reversion due to a somatic second-site mutation in CARD11 deficiency.
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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name
Omenn syndrome associated with ...... mutation in CARD11 deficiency.
@ast
Omenn syndrome associated with ...... mutation in CARD11 deficiency.
@en
type
label
Omenn syndrome associated with ...... mutation in CARD11 deficiency.
@ast
Omenn syndrome associated with ...... mutation in CARD11 deficiency.
@en
prefLabel
Omenn syndrome associated with ...... mutation in CARD11 deficiency.
@ast
Omenn syndrome associated with ...... mutation in CARD11 deficiency.
@en
P2093
P2860
P50
P1433
P1476
Omenn syndrome associated with ...... mutation in CARD11 deficiency.
@en
P2093
Anne Rensing-Ehl
Brigitte Strahm
Christopher Goodnow
Klaus Schwarz
Marcus Krüger
Myriam R Lorenz
Paul Fisch
Philipp Henneke
Susan Farmand
P2860
P304
P356
10.1182/BLOOD-2015-03-631374
P407
P577
2015-08-19T00:00:00Z