Congenital IL-12R1β receptor deficiency and thrombophilia in a girl homozygous for an IL12RB1 mutation and compound heterozygous for MTFHR mutations: A case report and literature review.
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J. Casanova | J. Bustamante | S. Doğanay | B. Akyıldız | H. H. Akar | T. Patiroglu | O. Ceylan | M. Kose