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Alternative polyadenylation of MeCP2: Influence of cis-acting elements and trans-acting factors
The human MeCP 2 gene encodes a ubiquitously expressed methyl CpG binding protein. Mutations in this gene cause a neurodevelopmental disorder called Rett Syndrome (RS). Mutations identified in the coding region of MeCP 2 account for approximately 65% of all RS cases. However, 35% of all patients do...
Αποθηκεύτηκε σε:
| Κύριοι συγγραφείς: | , , , , , , |
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| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
2010
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4096559/ https://ncbi.nlm.nih.gov/pubmed/20400852 |
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