טוען...
Cacna1g is a genetic modifier of epilepsy in a mouse model of Dravet syndrome
Dravet syndrome, an early onset epileptic encephalopathy, is most often caused by de novo mutation of the neuronal voltage-gated sodium channel gene SCN1A. Mouse models with deletion of Scn1a recapitulate Dravet syndrome phenotypes, including spontaneous generalized tonic-clonic seizures, susceptibi...
שמור ב:
| הוצא לאור ב: | Epilepsia |
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| Main Authors: | , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
2017
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5554089/ https://ncbi.nlm.nih.gov/pubmed/28556246 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/epi.13811 |
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