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Volumn 45, Issue 1, 2008, Pages 278-282

Molecular genetic analysis of Hungarian patients with the hyper-immunoglobulin M syndrome

Author keywords

AID; CD40L; Hyper IgM syndrome

Indexed keywords

CD40 ANTIGEN; IMMUNOGLOBULIN A; IMMUNOGLOBULIN G; IMMUNOGLOBULIN M;

EID: 34548260858     PISSN: 01615890     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.molimm.2007.04.014     Document Type: Article
Times cited : (11)

References (10)
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  • 2
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    • A novel splice-site mutation in the CD40L gene in a patient with X-linked hyper-IgM syndrome
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    • Activation-induced cytidine deaminase: structure-function relationship as based on the study of mutants
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    • Genetically acquired class-switch recombination defects: the multi-faced hyper-IgM syndrome
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    • Molecular analysis of a large cohort of patients with the hyper-immunoglobulin M (IgM) syndrome
    • Lee W.I., Torgerson T.R., Schumacher M.J., Yel L., Zhu Q., and Ochs H.D. Molecular analysis of a large cohort of patients with the hyper-immunoglobulin M (IgM) syndrome. Blood 105 (2005) 1881-1890
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  • 10
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    • Mutation of the CD40 ligand and its effect on CD40 ligand expression in patients with X-linked hyper-IgM syndrome
    • Seyama K., Nonoyama S., Gangsaas I., Hollenbaugh D., Pabst H.F., Aruffo A., and Ochs H.D. Mutation of the CD40 ligand and its effect on CD40 ligand expression in patients with X-linked hyper-IgM syndrome. Blood 92 (1998) 2421-2434
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.