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Increased H3K9 methylation and impaired expression of Protocadherins are associated with the cognitive dysfunctions of the Kleefstra syndrome
Kleefstra syndrome, a disease with intellectual disability, autism spectrum disorders and other developmental defects is caused in humans by haploinsufficiency of EHMT1. Although EHMT1 and its paralog EHMT2 were shown to be histone methyltransferases responsible for deposition of the di-methylated H...
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Udgivet i: | Nucleic Acids Res |
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Main Authors: | , , , , , , , , , , , , , , |
Format: | Artigo |
Sprog: | Inglês |
Udgivet: |
Oxford University Press
2018
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Fag: | |
Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6007260/ https://ncbi.nlm.nih.gov/pubmed/29554304 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gky196 |
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