The role of SLC2A1 in early onset and childhood absence epilepsies.

Muhle, Hiltrud

The role of SLC2A1 in early onset and childhood absence epilepsies. [electronic resource] - Epilepsy research Jul 2013 - 229-33 p. digital

Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't

1872-6844

10.1016/j.eplepsyres.2012.11.004 doi


Adolescent
Age of Onset
Base Sequence
Cohort Studies
Early Diagnosis
Epilepsy, Absence--diagnosis
Female
Genetic Carrier Screening
Glucose Transporter Type 1--genetics
Humans
Male
Molecular Sequence Data
Mutation--genetics
Young Adult