(Q35696704)
Statements
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First de novo KCND3 mutation causes severe Kv4.3 channel dysfunction leading to early onset cerebellar ataxia, intellectual disability, oral apraxia and epilepsy (English)
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Rebecca Schüle
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Stephan Züchner
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Katrien Smets
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Anna Duarri
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Tine Deconinck
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Berten Ceulemans
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Bart P van de Warrenburg
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Michael Anthony Gonzalez
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Nathalie Van der Aa
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Peter De Jonghe
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Dineke S Verbeek
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Jonathan Baets
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21 July 2015
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16
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51
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21 July 2015
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Identifiers
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