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Structural investigation of Rett-inducing MeCP2 mutations()
X-ray structure of methyl-CpG binding domain (MBD) of MeCP2, an intrinsically disordered protein (IDP) involved in Rett syndrome, offers a rational basis for defining the spatial distribution for most of the sites where mutations responsible of Rett syndrome, RTT, occur. We have ascribed pathogenici...
Tallennettuna:
| Julkaisussa: | Genes Dis |
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| Päätekijät: | , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Chongqing Medical University
2018
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6411616/ https://ncbi.nlm.nih.gov/pubmed/30906830 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.gendis.2018.09.005 |
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