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SCN8A mutations in Chinese patients with early onset epileptic encephalopathy and benign infantile seizures
BACKGROUND: SCN8A mutations have recently been associated with epilepsy and neurodevelopmental disorders. This study aimed to broaden the phenotypic-spectrum of disease related with SCN8A mutations. METHODS: To identify the pathogenic gene of a Chinese family, in which six members suffered from epil...
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| Publicat a: | BMC Med Genet |
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| Autors principals: | , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2017
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5604297/ https://ncbi.nlm.nih.gov/pubmed/28923014 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12881-017-0460-1 |
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