DRAVET SYNDROME; DRVT

Literature (3)

Literature for OMIM 607208: DRAVET SYNDROME; DRVT

Xenbase Articles:
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Denotes literature images)

A functional null mutation of SCN1B in a patient with Dravet syndrome., Patino GA,Claes LR,Lopez-Santiago LF,Slat EA,Dondeti RS,Chen C,O'Malley HA,Miyazaki H,Nukina N,Oyama F,De Jonghe P,Isom LL,Gray CB, J Neurosci. August 26, 2009; 29(34):1529-2401.
Moving gating charges through the gating pore in a Kv channel voltage sensor., Lacroix JJ,Campos FV,Bezanilla F,Hyde HC, Proc Natl Acad Sci U S A. May 13, 2014; 111(19):1091-6490.
A novel GABAergic dysfunction in human Dravet syndrome., Ruffolo G,Roseti C,Thom M,Limatola C,Aronica E,Palma E,van Vliet EA,Cifelli P, Epilepsia. November 1, 2018; 59(11):1528-1167.

A functional null mutation of SCN1B in a patient with Dravet syndrome., Patino GA,Claes LR,Lopez-Santiago LF,Slat EA,Dondeti RS,Chen C,O'Malley HA,Miyazaki H,Nukina N,Oyama F,De Jonghe P,Isom LL,Gray CB, J Neurosci. August 26, 2009; 29(34):1529-2401.

Moving gating charges through the gating pore in a Kv channel voltage sensor., Lacroix JJ,Campos FV,Bezanilla F,Hyde HC, Proc Natl Acad Sci U S A. May 13, 2014; 111(19):1091-6490.

A novel GABAergic dysfunction in human Dravet syndrome., Ruffolo G,Roseti C,Thom M,Limatola C,Aronica E,Palma E,van Vliet EA,Cifelli P, Epilepsia. November 1, 2018; 59(11):1528-1167.