A plethora of SCN1A mutations: what can they tell us?
- PMID: 16059449
- PMCID: PMC1176321
- DOI: 10.1111/j.1535-7597.2005.05105.x
A plethora of SCN1A mutations: what can they tell us?
References
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- Sugawara T, Tsurubuchi Y, Fujiwara T, Mazaki-Miyazaki E, Nagata K, Montal M, Inoue Y, Yamakawa K. Nav1.1 channels with mutations of severe myoclonic epilepsy in infancy display attenuated currents. Epilepsy Res. 2003;54:201–207. - PubMed
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