טוען...
Identification of Arx targets unveils new candidates for controlling cortical interneuron migration and differentiation
Mutations in the homeobox transcription factor ARX have been found to be responsible for a wide spectrum of disorders extending from phenotypes with severe neuronal migration defects, such as lissencephaly, to mild forms of intellectual disabilities without apparent brain abnormalities, but with ass...
שמור ב:
| Main Authors: | , |
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| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Frontiers Research Foundation
2011
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3280452/ https://ncbi.nlm.nih.gov/pubmed/22355284 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fncel.2011.00028 |
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