Individualizing Treatment Approaches for Epileptic Patients with Glucose Transporter Type1 (GLUT-1) Deficiency

Monogenic and polygenic mutations are important contributors in patients suffering from epilepsy, including metabolic epilepsies which are inborn errors of metabolism with a good respond to specific dietetic treatments. Heterozygous variation in solute carrier family 2, facilitated glucose transport...

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Detalles Bibliográficos
Autores principales: Daci, Armond, Bozalija, Adnan, Jashari, Fisnik, Krasniqi, Shaip
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5796071/
https://www.ncbi.nlm.nih.gov/pubmed/29303961
http://dx.doi.org/10.3390/ijms19010122

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5796071/
https://www.ncbi.nlm.nih.gov/pubmed/29303961
http://dx.doi.org/10.3390/ijms19010122

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