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Author

Amina Saad-Djaballah

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2 papers indexed here

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Open access Oct 2026

MHC-II deficiency in a large Algerian cohort: Clinical, immunological, and genetic characterization

This study characterizes the clinical, immunological, and genetic spectrum of MHC-II deficiency in the largest cohort reported to date. It identifies recurrent and novel variants and reveals genotype–phenotype differences.

Lydia Lamara Mahammed, Brahim Belaid, Ko-On-Wing Chan et al. · 0 citations
Open access Oct 2026

The genetic landscape of RAG deficiency: Novel and founder variants in a large Algerian cohort

This study characterizes RAG1/RAG2 deficiency, a severe inherited immune disorder, in the largest reported cohort from a North African country. Two founder mutations explain most cases, yet limited transplant access drives high mortality, highlighting the need for newborn screening.

Brahim Belaid, Ko-On-Wing Chan, J. Stoddard et al. · 0 citations

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