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Glut1 deficiency is a rare but treatable cause of childhood absence epilepsy with atypical features

Document Type

Journal

Author

Soto-Insuga, Victor; Guerrero Lopez, Rosa; Losada-Del Pozo, Rebeca; Rodrigo-Moreno, Maria; Martinez Cayuelas, Elena; Giraldez, Beatriz G.; Diaz-Gomez, Ester; Sanchez-Martin, Gema; Olivie Garcia, Laura; Serratosa, Jose M.; GEGEI

Source

EPILEPSY RESEARCH; AUG 2019, 154 p39-p41, 3p.

Subject

Language

English

ISSN

18726844

Online Access

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

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