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Claes L, Del-Favero J, Ceulemans B, Lagae L, Van Broeckhoven C, De Jonghe P (2001)
De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy.
68
1327
32
2001
Am J Hum Genet
Other categories referring to Claes L, Del-Favero J, Ceulemans B, Lagae L, Van Broeckhoven C, De Jonghe P (2001)
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