ICF, an immunodeficiency syndrome: DNA methyltransferase 3B involvement, chromosome anomalies, and gene dysregulation
Author:
Publisher
Informa UK Limited
Subject
Immunology,Immunology and Allergy
Link
http://www.tandfonline.com/doi/pdf/10.1080/08916930802024202
Reference174 articles.
1. The ICF syndrome, a DNA methyltransferase 3B deficiency and immunodeficiency disease
2. The DNMT3B DNA methyltransferase gene is mutated in the ICF immunodeficiency syndrome
3. Assignment of cytosine-5 DNA methyltransferases Dnmt3a and Dnmt3b to mouse chromosome bands 12A2–A3 and 2H1 by in situ hybridization
4. Chromosome instability and immunodeficiency syndrome caused by mutations in a DNA methyltransferase gene
5. DNA methyltransferase 3B mutations linked to the ICF syndrome cause dysregulation of lymphogenesis genes
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