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Brain somatic mutations in MTOR leading to focal cortical dysplasia
Focal cortical dysplasia type II (FCDII) is a focal malformation of the developing cerebral cortex and the major cause of intractable epilepsy. However, since the molecular genetic etiology of FCD has remained enigmatic, the effective therapeutic target for this condition has remained poorly underst...
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| Publicado no: | BMB Rep |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Korean Society for Biochemistry and Molecular Biology
2016
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4915119/ https://ncbi.nlm.nih.gov/pubmed/26779999 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5483/BMBRep.2016.49.2.010 |
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