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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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| Autor principal: | |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Epilepsy Society
2001
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| Acesso em linha: | 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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