Publication | Open Access
Conditional Deletion of Foxg1 Alleviates Demyelination and Facilitates Remyelination via the Wnt Signaling Pathway in Cuprizone-Induced Demyelinated Mice
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2005 | 1.2K | |
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2008 | 844 | |
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Duplications of FOXG1 in 14q12 are associated with developmental epilepsy, mental retardation, and severe speech impairment Nicola Brunetti‐Pierri, Alex R. Paciorkowski, Roberto Ciccone, European Journal of Human Genetics Developmental BiologyMendelian DisorderSevere Speech ImpairmentGenetic DisorderGenetics | 2010 | 187 |
2011 | 185 | |
2006 | 184 | |
2009 | 151 |
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