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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Dades bibliogràfiques
Publicat a:Neuroimage Clin
Autors principals: 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.
Format: Artigo
Idioma:Inglês
Publicat: Elsevier 2018
Matèries:
Regular Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC6029499/
https://ncbi.nlm.nih.gov/pubmed/29984154
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nicl.2018.04.001
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