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

• CLAES L

収録刊行物

• Am J Hum Genet

  Am J Hum Genet 68 1327-1332, 2001

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• CRID: 1571135650912771840
• NII論文ID: 10025579819
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