Progressive myoclonus epilepsy caused by a gain-of-function KCNA2 mutation

Laura Canafoglia; Barbara Castellotti; Francesca Ragona; Elena Freri; Tiziana Granata; Luisa Chiapparini; Cinzia Gellera; Vidmer Scaioli; Silvana Franceschetti; Jacopo C. DiFrancesco

doi:10.1016/j.seizure.2019.01.005

Progressive myoclonus epilepsy caused by a gain-of-function KCNA2 mutation

Laura Canafoglia, Barbara Castellotti, Francesca Ragona, Elena Freri, Tiziana Granata, Luisa Chiapparini, Cinzia Gellera, Vidmer Scaioli, Silvana Franceschetti, Jacopo C. DiFrancesco

Fondazione IRCCS Istituto Neurologico "C. Besta"

Research output: Contribution to journal › Article › peer-review

Original language	English
Pages (from-to)	106-108
Number of pages	3
Journal	Seizure
Volume	65
DOIs	https://doi.org/10.1016/j.seizure.2019.01.005
Publication status	Published - Feb 1 2019

Keywords

Genetic ataxia
KCNA2 gene
Potassium channelopathy
Progressive myoclonus epilepsy

ASJC Scopus subject areas

Neurology
Clinical Neurology

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10.1016/j.seizure.2019.01.005

Cite this

@article{25bbacd7ad774023b89e590875fc3faf,

title = "Progressive myoclonus epilepsy caused by a gain-of-function KCNA2 mutation",

keywords = "Genetic ataxia, KCNA2 gene, Potassium channelopathy, Progressive myoclonus epilepsy",

author = "Laura Canafoglia and Barbara Castellotti and Francesca Ragona and Elena Freri and Tiziana Granata and Luisa Chiapparini and Cinzia Gellera and Vidmer Scaioli and Silvana Franceschetti and DiFrancesco, {Jacopo C.}",

year = "2019",

month = feb,

day = "1",

doi = "10.1016/j.seizure.2019.01.005",

language = "English",

volume = "65",

pages = "106--108",

journal = "Seizure : the journal of the British Epilepsy Association",

issn = "1059-1311",

publisher = "W.B. Saunders Ltd",

}

TY - JOUR

T1 - Progressive myoclonus epilepsy caused by a gain-of-function KCNA2 mutation

AU - Canafoglia, Laura

AU - Castellotti, Barbara

AU - Ragona, Francesca

AU - Freri, Elena

AU - Granata, Tiziana

AU - Chiapparini, Luisa

AU - Gellera, Cinzia

AU - Scaioli, Vidmer

AU - Franceschetti, Silvana

AU - DiFrancesco, Jacopo C.

PY - 2019/2/1

Y1 - 2019/2/1

KW - Genetic ataxia

KW - KCNA2 gene

KW - Potassium channelopathy

KW - Progressive myoclonus epilepsy

UR - http://www.scopus.com/inward/record.url?scp=85060095623&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=85060095623&partnerID=8YFLogxK

U2 - 10.1016/j.seizure.2019.01.005

DO - 10.1016/j.seizure.2019.01.005

M3 - Article

AN - SCOPUS:85060095623

VL - 65

SP - 106

EP - 108

JO - Seizure : the journal of the British Epilepsy Association

JF - Seizure : the journal of the British Epilepsy Association

SN - 1059-1311

ER -

Progressive myoclonus epilepsy caused by a gain-of-function KCNA2 mutation

Keywords

ASJC Scopus subject areas

Access to Document

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