The 752delG26 mutation in the RFXANK gene associated with major histocompatibility complex class II deficiency: evidence for a founder effect in the Moroccan population

por Naamane, H, Ailal, F, Abidi, O, Jeddane, L, Najib, J, Barakat, A, Bousfiha, AA
Publicado 2011

Research of anti-GAD and anti-IA2 autoantibodies by ELISA test in a series of Moroccan pediatric patients with diabetes type 1

por Belhiba, O, Aadam, Z, Jeddane, L, Saile, R, Salih ALJ, H, Bousfiha, AA, Jennane, F
Publicado 2020