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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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Bibliographic Details
Main Authors: Friocourt, Gaëlle, Parnavelas, John G.
Format: Artigo
Language:Inglês
Published: Frontiers Research Foundation 2011
Subjects:
Online Access: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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