Table 1_Case Report: A novel CIITA mutation causing MHC class II deficiency: first reported case in Morocco.pdf

Table 1_Case Report: A novel CIITA mutation causing MHC class II deficiency: first reported case in Morocco.pdf

<p>Major histocompatibility complex class II (MHC II) deficiency (bare lymphocyte syndrome type II) is an autosomal-recessive combined immunodeficiency caused by pathogenic variants in the transcriptional regulators CIITA, RFXANK, RFX5, or RFXAP. While RFXANK founder mutations predominate in N...

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Dades bibliogràfiques
Autor principal: Aziza Bachir Kattra (22678628) (author)
Altres autors: Fatima Ailal (385550) (author), Ibtihal Benhsaien (21684503) (author), Mohammed Fahi (22678631) (author), Asmaa Drissi Bourhanbour (22678634) (author), Ahamada Elamine (22678637) (author), Zahra Aadam (22678640) (author), Abderrahmane Errami (19686109) (author), Ahmed Aziz Bousfiha (21684512) (author), Jalila El Bakkouri (10098387) (author)
Publicat: 2025
Matèries:
Genetic Immunology
major histocompatibility complex class II deficiency
CIITA gene
bare lymphocyte syndrome (BLS)
lymphopenia CD4
HLA-DR expression
consanguinity
Morocco
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