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Mutation in the KCNQ2 gene - a rare cause for Rolandic epilepsy

Document Type

Journal

Author

Aleksandrova, I.; Bojinova-Tchamova, V.; Ivanova, N.; Slavkova, E.; Dimova, P.; Pejcheva, V.; Kamenarova, K.; Kuneva, R.; Jordanova, A.

Source

EUROPEAN JOURNAL OF NEUROLOGY; JUN 2015, 22 p240-p240, 1p. Supplement: 1

Subject

Language

English

ISSN

14681331

Online Access

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

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