Related references
Note: Only part of the references are listed.The same mutation in a family with adenosine deaminase 2 deficiency
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Hematopoietic stem cell transplantation rescues the hematological, immunological, and vascular phenotype in DADA2
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ADA2 deficiency (DADA2) as an unrecognised cause of early onset polyarteritis nodosa and stroke: a multicentre national study
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Adenosine deaminase type 2 deficiency masquerading as GATA2 deficiency: Successful hematopoietic stem cell transplantation
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IL-17 receptor A and adenosine deaminase 2 deficiency in siblings with recurrent infections and chronic inflammation
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EUROPEAN JOURNAL OF PEDIATRICS (2014)
Early- Onset Stroke and Vasculopathy Associated with Mutations in ADA2
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NEW ENGLAND JOURNAL OF MEDICINE (2014)
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Mutations in CECR1 associated with a neutrophil signature in peripheral blood
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Dependence of Immunoglobulin Class Switch Recombination in B Cells on Vesicular Release of ATP and CD73 Ectonucleotidase Activity
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Regulation of inflammation by adenosine
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FRONTIERS IN IMMUNOLOGY (2013)
Structural Basis for the Growth Factor Activity of Human Adenosine Deaminase ADA2
Anton V. Zavialov et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2010)
Human adenosine deaminase 2 induces differentiation of monocytes into macrophages and stimulates proliferation of T helper cells and macrophages
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JOURNAL OF LEUKOCYTE BIOLOGY (2010)
INFEVERS: the Registry for FMF and hereditary inflammatory disorders mutations
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