Understanding the Spectrum of SLC2A1-Associated Disorders
Investigators from the Danish Epilepsy Center the frequency of SLC2A1 mutations in a cohort of patients with different types of epilepsies.
Main Authors: | , |
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Format: | Article |
Language: | English |
Published: |
Pediatric Neurology Briefs Publishers
2017-02-01
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Series: | Pediatric Neurology Briefs |
Subjects: | |
Online Access: | https://www.pediatricneurologybriefs.com/articles/3798 |