De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy (Q35235370)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy |
scientific article |
Statements
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De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy (English)
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Anna-Elina Lehesjoki
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Ludger Schöls
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Sarah Weckhuysen
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Wieland Kiess
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Aarno Palotie
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Rebecca Schüle
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Stephan Züchner
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Dorota Hoffman-Zacharska
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Steffen Syrbe
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Ulrike B S Hedrich
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Erik Riesch
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Tania Djémié
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Stephan Müller
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Laura Hernandez-Hernandez
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Hande S Caglayan
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Mutluay Arslan
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José M Serratosa
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Heidrun Löffler
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Katja Detert
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Thomas Dorn
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Heinrich Vogt
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Günter Krämer
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Primus E Mullis
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Tarja Linnankivi
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Katalin Sterbova
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Christian M Korff
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Yvonne G Weber
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Maja Steinlin
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Sabina Gallati
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Matthias K Bernhard
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Andreas Merkenschlager
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EuroEPINOMICS RES consortium
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Michael Gonzalez
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Arvid Suls
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Peter De Jonghe
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Ingo Helbig
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Saskia Biskup
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Markus Wolff
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Snezana Maljevic
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Sanjay M Sisodiya
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Holger Lerche
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Johannes R Lemke
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9 March 2015
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47
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4
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393-399
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Identifiers
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