Major histocompatibility complex class II expression deficiency caused by a RFXANK founder mutation: a survey of 35 patients
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author: Laurent Abel, Jean-Laurent Casanova, Capucine Picard, Marianne Debré, Quentin B Vincent, Julie Bruneau, Fabien Touzot, Danielle Canioni, Stéphane Blanche, Ahmed Aziz Bousfiha, Pierre Frange, Alain Fischer
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