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European Journal of Microbiology & Immunology|March 29, 2014
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 reviewH H Akar, M Kose, O Ceylan, et al.Journal of Nephrology|September 24, 1999
Carotid intima-media thickness and ACE-gene polymorphism in hemodialysis patientsG Nergizoğlu, K Keven, M A Gürses, et al.Pageof 3