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Role of cytoskeletal abnormalities in the neuropathology and pathophysiology of type I lissencephaly

Type I lissencephaly or agyria-pachygyria is a rare developmental disorder which results from a defect of neuronal migration. It is characterized by the absence of gyri and a thickening of the cerebral cortex and can be associated with other brain and visceral anomalies. Since the discovery of the f...

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Detalles Bibliográficos
Main Authors: Friocourt, Gaëlle, Marcorelles, Pascale, Saugier-Veber, Pascale, Quille, Marie-Lise, Marret, Stephane, Laquerrière, Annie
Formato: Artigo
Idioma:Inglês
Publicado: Springer-Verlag 2010
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC3037170/
https://ncbi.nlm.nih.gov/pubmed/21046408
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00401-010-0768-9
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