Basal ganglia involvement in ARX patients: The reason for ARX patients very specific grasping?

The ARX (Aristaless Related homeoboX) gene was identified in 2002 as responsible for XLAG syndrome, a lissencephaly characterized by an almost complete absence of cortical GABAergic interneurons, and for milder forms of X-linked Intellectual Disability (ID) without apparent brain abnormalities. The...

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Detalles Bibliográficos
Autores principales: Curie, Aurore, Friocourt, Gaëlle, des Portes, Vincent, Roy, Alice, Nazir, Tatjana, Brun, Amandine, Cheylus, Anne, Marcorelles, Pascale, Retzepi, Kalliroi, Maleki, Nasim, Bussy, Gérald, Paulignan, Yves, Reboul, Anne, Ibarrola, Danielle, Kong, Jian, Hadjikhani, Nouchine, Laquerrière, Annie, Gollub, Randy L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Regular Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6029499/
https://www.ncbi.nlm.nih.gov/pubmed/29984154
http://dx.doi.org/10.1016/j.nicl.2018.04.001

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6029499/
https://www.ncbi.nlm.nih.gov/pubmed/29984154
http://dx.doi.org/10.1016/j.nicl.2018.04.001

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