Alu-repeat-induced deletions within the NCF2 gene causing p67-phox-deficient chronic granulomatous disease (CGD).
type: Dataset
description: International audience
issued: 2026-05-11T05:12:39.097951
language: en
modified: 2026-05-11T05:12:39.097958
contact point: Organization
  fn: CCSD
keyword: immunodeficiency
keyword: infoeu-reposemanticsarticle
keyword: journal-articles
keyword: mesh-alu-elements
keyword: mesh-base-sequence
keyword: mesh-cell-line
keyword: mesh-exons
keyword: mesh-gene-expression-regulation
keyword: mesh-granulomatous-disease-chronic
keyword: mesh-half-life
keyword: mesh-humans
keyword: mesh-molecular-sequence-data
keyword: mesh-mutant-proteins
keyword: mesh-nadph-oxidase
keyword: mesh-phosphoproteins
keyword: mesh-protein-stability
keyword: mesh-protein-structure-secondary
keyword: mesh-reactive-oxygen-species
keyword: mesh-recombination-genetic
keyword: mesh-rna-messenger
keyword: mesh-rna-stability
keyword: mesh-sequence-deletion
keyword: ncf2
keyword: phagocyte
keyword: recombination
keyword: sdvimmiilife-sciences-q-bioimmunologyinnate-immunity
landing page: 1059-7794

Alu-repeat-induced deletions within the NCF2 gene causing p67-phox-deficient chronic granulomatous disease (CGD).
type: Distribution
format: HTML
issued: 2026-05-11T05:12:39.129165
modified: 2026-05-11T05:12:39.068442
access URL: https://hal.science/hal-00820713

test_moissonnage_selune
type: Agent