(Q34122789)
Statements
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Frequent mutations of SCN1A in severe myoclonic epilepsy in infancy (English)
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Sugawara T
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Mazaki-Miyazaki E
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Fukushima K
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Shimomura J
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Fujiwara T
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Hamano S
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Inoue Y
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Yamakawa K
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1 April 2002
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58
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1122-1124
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Identifiers
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1 reference