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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...
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| Hlavní autoři: | , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Frontiers Research Foundation
2011
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| Témata: | |
| On-line přístup: | 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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