SCN1A (2528delG) novel truncating mutation with benign outcome of severe myoclonic epilepsy of infancy (Q82676480)
scientific article published on 01 February 2006
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Current Data About SCN1A (2528delG) novel truncating mutation with benign outcome of severe myoclonic epilepsy of infancy
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(P1476) "SCN1A (2528delG) novel truncating mutation with benign outcome of severe myoclonic epilepsy of infancy" (language: en)
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(P2093) Buoni S
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Orrico A
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Galli L
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Zannolli R
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Burroni L
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Fois A
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other details
description scientific article published on 01 February 2006

External Links
(P356) 10.1212/01.WNL.0000198504.41315.B1
(P698) 16505326