טוען...
Chd7 Cooperates with Sox10 and Regulates the Onset of CNS Myelination and Remyelination
Mutations in CHD7, encoding ATP-dependent chromodomain-helicase-DNA-binding protein 7, in CHARGE syndrome leads to multiple congenital anomalies including craniofacial malformations, neurological dysfunction and growth delay. Currently, mechanisms underlying the CNS phenotypes remain poorly understo...
שמור ב:
| הוצא לאור ב: | Nat Neurosci |
|---|---|
| Main Authors: | , , , , , , , , , , , , , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
2016
|
| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4846514/ https://ncbi.nlm.nih.gov/pubmed/26928066 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/nn.4258 |
| תגים: |
הוספת תג
אין תגיות, היה/י הראשונ/ה לתייג את הרשומה!
|