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Two Novel KCNQ2 Mutations in 2 Families With Benign Familial Neonatal Convulsions
Benign familial neonatal convulsion is a rare autosomal dominant inherited epilepsy syndrome characterized by unprovoked seizures in the first few days of life, normal psychomotor development, and a positive intergenerational family history of neonatal seizures. Over 90% of the affected individuals...
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| Publicado no: | Child Neurol Open |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
SAGE Publications
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5417349/ https://ncbi.nlm.nih.gov/pubmed/28503627 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1177/2329048X17691396 |
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