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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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Библиографические подробности
Главный автор: Crino, Peter B.
Формат: Artigo
Язык:Inglês
Опубликовано: American Epilepsy Society 2001
Предметы:
Online-ссылка: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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