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Mutations in SCN2A are an emerging cause of early onset epilepsy

Document Type

Academic Journal

Author

MCTAGUE, A; ELTZE, C; MOELLER, F; TRUMP, N; SCOTT, R H; CHONG, K; CHOW, G; GISSEN, P; HURST, J A; PAPANDREOU, A; PATEL, J; VARADKAR, S; WHITNEY, A; CROSS, J H; KURIAN, M A

Source

Developmental Medicine & Child Neurology. Jan 01, 2015 57 Suppl 1:3-4

Subject

Language

English

ISSN

0012-1622

Online Access

Full Text (Wiley Journals) Full Text (Wiley-DB) Web of Science JCR 저널정보 Find it@PNU

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