CORE
🇺🇦Â
 make metadata, not war
Services
Services overview
Explore all CORE services
Access to raw data
API
Dataset
FastSync
Content discovery
Recommender
Discovery
OAI identifiers
OAI Resolver
Managing content
Dashboard
Bespoke contracts
Consultancy services
Support us
Support us
Membership
Sponsorship
Community governance
Advisory Board
Board of supporters
Research network
About
About us
Our mission
Team
Blog
FAQs
Contact us
Filters
1 research outputs found
Three novel SLC2A1 mutations in Bulgarian patients with different forms of genetic generalized epilepsy reflecting the clinical and genetic diversity of GLUT1-deficiency syndrome
Author
Aleksandrova Iliana
Bozhinova Veneta
+14Â more
Dimova Petya
Hristova Dimitrina
Ivanova Nevyana
Jordanova Albena
Kamenarova Kunka
Kancheva Dalia
Kaneva Radka
Litvinenko Ivan
Mitev Vanio
Peycheva Valentina
Sarailieva Gergana
Todorova Diana
Tomov Veselin
Tsekova Irina
Publication venue
Publication date
01/01/2018
Field of study
No full text
Institutional Repository Universiteit Antwerpen