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Deletions or duplications in KCNQ2 can cause benign familial neonatal seizures
BACKGROUND: Benign familial neonatal seizures are most often caused by mutations in the voltage‐gated potassium channel subunit gene KCNQ2. More than 60 mutations have been described in BFNS families, approximately half of which lead to protein truncation. The hypothesis of this study was that delet...
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| Autors principals: | , , , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BMJ Group
2007
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2652819/ https://ncbi.nlm.nih.gov/pubmed/17675531 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2007.051938 |
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