Nocturnal frontal lobe epilepsy (NFLE) can be sporadic or autosomal dominant; some families have nicotinic acetylcholine receptor subunit mutations. We report a novel autosomal recessive phenotype in a single family and identify the causative gene.

PRIMA1 mutation: a new cause of nocturnal frontal lobe epilepsy / Hildebrand, M.S., Tankard, R., Gazina, E.V., Damiano, J.A., Lawrence, K.M., Dahl, H.M., Regan, B.M., Shearer, A.E., Smith, R.J.H., Marini, C., Guerrini, R., Labate, A., Gambardella, A., Tinuper, P., Lichetta, L., Baldassari, S., Bisulli, F., Pippucci, T., Scheffer, I.E., Reid, C.A., et al.. - In: ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY. - ISSN 2328-9503. - STAMPA. - 2:(2015), pp. 821-30-830. [10.1002/acn3.224]

PRIMA1 mutation: a new cause of nocturnal frontal lobe epilepsy

Marini, Carla;GUERRINI, RENZO;
2015

Abstract

Nocturnal frontal lobe epilepsy (NFLE) can be sporadic or autosomal dominant; some families have nicotinic acetylcholine receptor subunit mutations. We report a novel autosomal recessive phenotype in a single family and identify the causative gene.
2015
2
821-30
830
Hildebrand, Michael S; Tankard, Rick; Gazina, Elena V; Damiano, John A; Lawrence, Kate M; Dahl, Hans-Henrik M; Regan, Brigid M; Shearer, Aiden Eliot; ...espandi
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/1017158
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