(Q39642644)
Statements
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SCN2A mutation associated with neonatal epilepsy, late-onset episodic ataxia, myoclonus, and pain (English)
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Y Liao
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A-K Anttonen
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E Liukkonen
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E Gaily
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S Maljevic
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S Schubert
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A Bellan-Koch
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S Petrou
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V E Ahonen
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H Lerche
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A-E Lehesjoki
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1 October 2010
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75
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16
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1454-1458
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Identifiers
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