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The histone methyltransferase MMSET regulates class-switch recombination
Wolf-Hirschhorn syndrome (WHS) is a genetic disease with characteristic facial features and developmental disorders. Of interest, loss of the MMSET gene (also known as WHSC1) is considered to be responsible for the core phenotypes of this disease. Patients with WHS also display antibody deficiency,...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3775478/ https://ncbi.nlm.nih.gov/pubmed/23241889 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4049/jimmunol.1201811 |
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