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Fine Mapping of an Epilepsy Modifier Gene on Mouse Chromosome 19
Mutations in voltage-gated sodium channels are associated with several types of human epilepsy. Variable expressivity and penetrance are common features of inherited epilepsy caused by sodium channel mutations, suggesting that genetic modifiers may influence clinical severity. The mouse model Scn2a(...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2009
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2804848/ https://ncbi.nlm.nih.gov/pubmed/19513789 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00335-009-9193-6 |
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