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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Detalhes bibliográficos
Publicado no:Neuroimage Clin
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: Elsevier 2018
Assuntos:
Regular Article
Acesso em linha: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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