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Investigating the genetic basis of fever-associated syndromic epilepsies using copy number variation analysis
Fever-associated syndromic epilepsies ranging from febrile seizures plus (FS+) to Dravet syndrome have a significant genetic component. However, apart from SCN1A mutations in over 80% of patients with Dravet syndrome, the genetic underpinnings of these epilepsies remain largely unknown. Therefore, w...
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| Foilsithe in: | Epilepsia |
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| Main Authors: | , , , , , , , , , , , , |
| Formáid: | Artigo |
| Teanga: | Inglês |
| Foilsithe: |
2015
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| Ábhair: | |
| Rochtain Ar Líne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4363163/ https://ncbi.nlm.nih.gov/pubmed/25690317 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/epi.12920 |
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