De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy (Q24533495)
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Current Data About De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy
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(P1932) C Van Broeckhoven

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(P1476) "De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy" (language: en)

(P2093) 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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P De Jonghe
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(P813) Wednesday, May 30, 2018