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A mutation in the neonatal isoform of SCN2A causes neonatal-onset epilepsy

Document Type

Journal

Author

Penkl, Anja; Reunert, Janine; Debus, Otfried M.; Homann, Anna; Och, Ulrike; Rust, Stephan; Marquardt, Thorsten

Source

AMERICAN JOURNAL OF MEDICAL GENETICS PART A; DEC 7 2021, 7p.

Subject

Language

English

ISSN

15524833

Online Access

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

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