The DNMT3B DNA methyltransferase gene is mutated in the ICF immunodeficiency syndrome
Author:
Publisher
Proceedings of the National Academy of Sciences
Subject
Multidisciplinary
Reference40 articles.
1. Multibranched chromosomes 1, 9, and 16 in a patient with combined IgA and IgE deficiency
2. An embryonic-like methylation pattern of classical satellite DNA is observed in ICF syndrome
3. DNA demethylation and pericentromeric rearrangements of chromosome 1
4. α-Satellite DNA methylation in normal individuals and in ICF patients: heterogeneous methylation of constitutive heterochromatin in adult and fetal tissues
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