A functional null mutation of SCN1B in a patient with Dravet syndrome.
Bibliographic Information
- Title
- A functional null mutation of SCN1B in a patient with Dravet syndrome.
- Author
- Patino G.A., Claes L.R., Lopez-Santiago L.F., Slat E.A., Dondeti R.S., Chen C., O'Malley H.A., Gray C.B., Miyazaki H., Nukina N., Oyama F., De Jonghe P., Isom L.L.
Journal
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- J.Neurosci. 29
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J.Neurosci. 29 10764-10778, 2009
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Details 詳細情報について
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- CRID
- 1010000782039528321
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- Article Type
- journal article
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- Data Source
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- KAKEN