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Recurrent de novo mutations of SCN1A in severe myoclonic epilepsy of infancy

Document Type

Journal

Author

Kearney, JA; Wiste, AK; Stephani, U; Trudeau, MM; Siegel, A; RamachandranNair, R; Elterman, RD; Muhle, H; Reinsdorf, S; Shields, WD; Meisler, MH; Escayg, A

Source

PEDIATRIC NEUROLOGY; FEB 2006, 34 2, p116-p120, 5p.

Subject

Language

English

ISSN

08878994

Online Access

Full Text (ScienceDirect 종량제) Web of Science JCR 저널정보 Scopus Find it@PNU

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