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Understanding the Spectrum of SLC2A1-Associated Disorders
Investigators from the Danish Epilepsy Center the frequency of SLC2A1 mutations in a cohort of patients with different types of epilepsies.
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Pediatric Neurology Briefs Publishers
2017
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5405020/ https://www.ncbi.nlm.nih.gov/pubmed/28507422 http://dx.doi.org/10.15844/pedneurbriefs-31-2-1 |