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Article

SCN1A (2528delG) novel truncating mutation with benign outcome of severe myoclonic epilepsy of infancy.

Neurology - 28 Feb 2006

Buoni S, Orrico A, Galli L, Zannolli R, Burroni L, Hayek J, Fois A, Sorrentino V

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Share to Electroencephalography
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 16505326
DOI: 10.1212/01.WNL.0000198504.41315.B1

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