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Reelin' in Genes for Cortical Dysplasia

Malformations of cortical development are a broad family of disorders that are characterized by abnormal cytoarchitecture of the cerebral cortex and a high association with epilepsy. In recent years positional cloning strategies have been implemented to identify several distinct gene mutations that...

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Bibliografske podrobnosti
Glavni avtor: Crino, Peter B.
Format: Artigo
Jezik:Inglês
Izdano: American Epilepsy Society 2001
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC320819/
https://ncbi.nlm.nih.gov/pubmed/15309192
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1046/j.1535-7597.2001.00014.x
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