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Activation-induced cytidine deaminase (AID) deficiency causes the autosomal recessive form of the Hyper-IgM syndrome (HIGM2).
Revy P, Muto T, Levy Y, Geissmann F, Plebani A, Sanal O, Catalan N, Forveille M, Dufourcq-Labelouse R, Gennery A, Tezcan I, Ersoy F, Kayserili H, Ugazio AG, Brousse N, Muramatsu M, Notarangelo LD, Kinoshita K, Honjo T, Fischer A, Durandy A. Revy P, et al. Among authors: ersoy f. Cell. 2000 Sep 1;102(5):565-75. doi: 10.1016/s0092-8674(00)00079-9. Cell. 2000. PMID: 11007475 Free article.
Two genes are responsible for Griscelli syndrome at the same 15q21 locus.
Pastural E, Ersoy F, Yalman N, Wulffraat N, Grillo E, Ozkinay F, Tezcan I, Gediköglu G, Philippe N, Fischer A, de Saint Basile G. Pastural E, et al. Among authors: ersoy f. Genomics. 2000 Feb 1;63(3):299-306. doi: 10.1006/geno.1999.6081. Genomics. 2000. PMID: 10704277
Mutations of chronic granulomatous disease in Turkish families.
Köker MY, Sanal O, De Boer M, Tezcan I, Metin A, Ersoy F, Roos D. Köker MY, et al. Among authors: ersoy f. Eur J Clin Invest. 2007 Jul;37(7):589-95. doi: 10.1111/j.1365-2362.2007.01828.x. Eur J Clin Invest. 2007. PMID: 17576211
Hyper-IgE syndrome: a case report.
Sanal O, Göçmen A, Tezcan I, Ersoy F, Adalioğlu G. Sanal O, et al. Among authors: ersoy f. Turk J Pediatr. 1990 Oct-Dec;32(4):273-8. Turk J Pediatr. 1990. PMID: 2135680
235 results