Doublecortin mutation leads to persistent defects in the Golgi apparatus and mitochondria in adult hippocampal pyramidal cells

Human doublecortin (DCX) mutations are associated with severe brain malformations leading to aberrant neuron positioning (heterotopia), intellectual disability and epilepsy. DCX is a microtubule-associated protein which plays a key role during neurodevelopment in neuronal migration and differentiati...

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מידע ביבליוגרפי

Principais autores:	M.A. Stouffer, R. Khalaf-Nazzal, C. Cifuentes-Diaz, G. Albertini, E. Bandet, G. Grannec, V. Lavilla, J.-F. Deleuze, R. Olaso, M. Nosten-Bertrand, F. Francis
פורמט:	Artigo
שפה:	Inglês
יצא לאור:	Elsevier 2022-06-01
סדרה:	Neurobiology of Disease
נושאים:	Cortical malformation Neurodevelopmental disorder Mouse knockout hippocampus Molecular and cellular analysis Morphology
גישה מקוונת:	http://www.sciencedirect.com/science/article/pii/S0969996122000948
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