A functional null mutation of SCN1B in a patient with Dravet syndrome.
書誌事項
- タイトル
- A functional null mutation of SCN1B in a patient with Dravet syndrome.
- 著者
- 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.
収録刊行物
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- J.Neurosci. 29
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J.Neurosci. 29 10764-10778, 2009