ARX polyalanine expansion mutations lead to migration impediment in the rostral cortex coupled with a developmental deficit of calbindin-positive cortical GABAergic interneurons

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dc.contributor.authorLee, K.
dc.contributor.authorIreland, K.
dc.contributor.authorBleeze, M.
dc.contributor.authorShoubridge, C.
dc.date.issued2017
dc.description.abstractAbstract not available
dc.description.statementofresponsibilityK. Lee, K. Ireland, M. Bleeze and C. Shoubridge
dc.identifier.citationNeuroscience, 2017; 357:220-231
dc.identifier.doi10.1016/j.neuroscience.2017.06.010
dc.identifier.issn0306-4522
dc.identifier.issn1873-7544
dc.identifier.orcidShoubridge, C. [0000-0002-0157-3084]
dc.identifier.urihttp://hdl.handle.net/2440/107488
dc.language.isoen
dc.publisherElsevier BV
dc.relation.granthttp://purl.org/au-research/grants/nhmrc/1063025
dc.relation.granthttp://purl.org/au-research/grants/arc/FT120100086
dc.rights© 2017 IBRO. Published by Elsevier Ltd. All rights reserved.
dc.source.urihttps://doi.org/10.1016/j.neuroscience.2017.06.010
dc.subjectARX; intellectual disability; epilepsy; interneuron migration; calbindin interneurons; polyalanine expansion mutations
dc.titleARX polyalanine expansion mutations lead to migration impediment in the rostral cortex coupled with a developmental deficit of calbindin-positive cortical GABAergic interneurons
dc.typeJournal article
pubs.publication-statusPublished

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