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

Hamid Naamane, Ouafaa El Maataoui, Fatima Ailal, Abdelhamid Barakat, Siham Bennani, J. Najib, Mohammed Hassar, Ahmed Aziz Bousfiha

European Journal of Pediatrics · 2010 · 39 citations · 29 references

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