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Dominant SCN2A Mutation Causes Familial Episodic Ataxia and Impairment of Speech Development

Document Type

Article

Author

Fazeli, W.; Becker, K.; Herkenrath, P.; Düchting, C.; Koy, A.; Cirak, S.; Liebau, M.C.; Körber, F.; Landgraf, P.; Simon, T.; Nürnberg, P.; Altmüller, J.; Thiele, H.; Dötsch, J.

Source

In: Neuropediatrics. (Neuropediatrics, 2018, 49(6):379-384)

Subject

Language

English

ISSN

14391899
0174304X

Online Access

Web of Science JCR 저널정보 Scopus Find it@PNU

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