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A Computational Model of the LGI1 Protein Suggests a Common Binding Site for ADAM Proteins
Mutations of human leucine-rich glioma inactivated (LGI1) gene encoding the epitempin protein cause autosomal dominant temporal lateral epilepsy (ADTLE), a rare familial partial epileptic syndrome. The LGI1 gene seems to have a role on the transmission of neuronal messages but the exact molecular me...
| Autores principales: | , , , , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
Public Library of Science
2011
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3066209/ https://www.ncbi.nlm.nih.gov/pubmed/21479274 http://dx.doi.org/10.1371/journal.pone.0018142 |