New genetic discoveries and primary immune deficiencies.

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Primary immunodeficiencies associated with eosinophilia Recurrent Pneumonia in Children: A Reasoned Diagnostic Approach and a Single Centre Experience.Autoimmunity in 2014.

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New genetic discoveries and primary immune deficiencies.

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article scientifique

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New genetic discoveries and primary immune deficiencies.

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New genetic discoveries and primary immune deficiencies.

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New genetic discoveries and primary immune deficiencies.

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New genetic discoveries and primary immune deficiencies.

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Vivian Hernandez-Trujillo

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Cernunnos, a novel nonhomologous end-joining factor, is mutated in human immunodeficiency with microcephaly

Genetics of SCID

Hyper-IgE syndrome with recurrent infections--an autosomal dominant multisystem disorder

Mutations in genes required for T-cell development: IL7R, CD45, IL2RG, JAK3, RAG1, RAG2, ARTEMIS, and ADA and severe combined immunodeficiency: HuGE review

STAT3 mutations in the hyper-IgE syndrome

Herpes simplex virus encephalitis in human UNC-93B deficiency

The actin regulator coronin 1A is mutant in a thymic egress-deficient mouse strain and in a patient with severe combined immunodeficiency.

Impaired T(H)17 cell differentiation in subjects with autosomal dominant hyper-IgE syndrome

Large deletions and point mutations involving the dedicator of cytokinesis 8 (DOCK8) in the autosomal-recessive form of hyper-IgE syndrome.

Autoantibodies against IL-17A, IL-17F, and IL-22 in patients with chronic mucocutaneous candidiasis and autoimmune polyendocrine syndrome type I

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s12016-013-8380-0

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145-153

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scholarly article

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10.1007/S12016-013-8380-0

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2014-04-01T00:00:00Z

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1016497522

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23860595

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New genetic discoveries and primary immune deficiencies.

about

P2860

P2860

New genetic discoveries and primary immune deficiencies.

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type

label

prefLabel

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P577

P6179

P698

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P577

P6179

P698