Frequent mutations of SCN1A in severe myoclonic epilepsy in infancy (Q34122789)
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(P577) Monday, April 1, 2002
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(P1476) "Frequent mutations of SCN1A in severe myoclonic epilepsy in infancy" (language: en)
(P2093) Sugawara T
Mazaki-Miyazaki E
Fukushima K
Shimomura J
Fujiwara T
Hamano S
Inoue Y
Yamakawa K
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