De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy (Q24533495)

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De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy
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    De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy (English)
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    L Claes
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    J Del-Favero
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    B Ceulemans
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    L Lagae
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    C Van Broeckhoven
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    P De Jonghe
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    June 2001
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    68
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    1327-32
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    6
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