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PP 72 Hematologic manifestations associated with deficiency of adenosine  deaminase 2 and a novel ada2 variant E. Hanafy*, M. Al
PP 72 Hematologic manifestations associated with deficiency of adenosine deaminase 2 and a novel ada2 variant E. Hanafy*, M. Al

Role of adenosine deaminase 2 gene variants in pediatric deficiency of  adenosine deaminase 2: A structural biological approach Corrigendum in  /10.3892/mmr.2021.12128
Role of adenosine deaminase 2 gene variants in pediatric deficiency of adenosine deaminase 2: A structural biological approach Corrigendum in /10.3892/mmr.2021.12128

ADA2 deficiency: case report of a new phenotype and novel mutation in two  sisters | RMD Open
ADA2 deficiency: case report of a new phenotype and novel mutation in two sisters | RMD Open

Electropherograms showing homozygous c.1358A>G pathogenic variant in... |  Download Scientific Diagram
Electropherograms showing homozygous c.1358A>G pathogenic variant in... | Download Scientific Diagram

ADA2 gene
ADA2 gene

Recombinant Human CECR1 protein (ABIN1349092)
Recombinant Human CECR1 protein (ABIN1349092)

Recombinant Human Adenosine Deaminase 2/CECR1 His Protein (NBP2-52348):  Novus Biologicals
Recombinant Human Adenosine Deaminase 2/CECR1 His Protein (NBP2-52348): Novus Biologicals

CECR1-mediated cross talk between macrophages and vascular mural cells  promotes neovascularization in malignant glioma | Oncogene
CECR1-mediated cross talk between macrophages and vascular mural cells promotes neovascularization in malignant glioma | Oncogene

The Many Faces of a Monogenic Autoinflammatory Disease: Adenosine Deaminase  2 Deficiency. - Abstract - Europe PMC
The Many Faces of a Monogenic Autoinflammatory Disease: Adenosine Deaminase 2 Deficiency. - Abstract - Europe PMC

Monogenic polyarteritis: the lesson of ADA2 deficiency | Pediatric  Rheumatology | Full Text
Monogenic polyarteritis: the lesson of ADA2 deficiency | Pediatric Rheumatology | Full Text

CECR1 - Wikipedia
CECR1 - Wikipedia

CECR1 - Wikipedia
CECR1 - Wikipedia

Mutations in CECR1 associated with a neutrophil signature in peripheral  blood | Pediatric Rheumatology | Full Text
Mutations in CECR1 associated with a neutrophil signature in peripheral blood | Pediatric Rheumatology | Full Text

Infevers - Statistics
Infevers - Statistics

CECR1 mutations so far detected | Download Table
CECR1 mutations so far detected | Download Table

Human Adenosine Deaminase 2/CECR1 ELISA Kit (Colorimetric) (NBP2-75221):  Novus Biologicals
Human Adenosine Deaminase 2/CECR1 ELISA Kit (Colorimetric) (NBP2-75221): Novus Biologicals

CECR1 - Wikipedia
CECR1 - Wikipedia

CECR1 Antibody(ABIN2782907)
CECR1 Antibody(ABIN2782907)

Cureus | A Rare Genetic Mutation Leading to a Deficiency of Adenosine  Deaminase 2 Enzyme in a Long-Standing Case of Cutaneous Polyarteritis  Nodosa: A Case Report | Media
Cureus | A Rare Genetic Mutation Leading to a Deficiency of Adenosine Deaminase 2 Enzyme in a Long-Standing Case of Cutaneous Polyarteritis Nodosa: A Case Report | Media

ADA2 Gene - GeneCards | ADA2 Protein | ADA2 Antibody
ADA2 Gene - GeneCards | ADA2 Protein | ADA2 Antibody

Behçet's disease and genetic interactions between HLA-B*51 and variants in  genes of autoinflammatory syndromes | Scientific Reports
Behçet's disease and genetic interactions between HLA-B*51 and variants in genes of autoinflammatory syndromes | Scientific Reports

RCSB PDB - 3LGD: Crystal structure of human adenosine deaminase growth  factor, adenosine deaminase type 2 (ADA2)
RCSB PDB - 3LGD: Crystal structure of human adenosine deaminase growth factor, adenosine deaminase type 2 (ADA2)

ADA2 Gene - GeneCards | ADA2 Protein | ADA2 Antibody
ADA2 Gene - GeneCards | ADA2 Protein | ADA2 Antibody

Gene sequencing in CECR1 gene. The patient had compound heterozygous... |  Download Scientific Diagram
Gene sequencing in CECR1 gene. The patient had compound heterozygous... | Download Scientific Diagram

Autoimmune phenotype with type I interferon signature in two brothers with  ADA2 deficiency carrying a novel CECR1 mutation | Pediatric Rheumatology |  Full Text
Autoimmune phenotype with type I interferon signature in two brothers with ADA2 deficiency carrying a novel CECR1 mutation | Pediatric Rheumatology | Full Text