Results 141 to 142 of about 1,836 (142)

Characterization of seizures and EEG findings in creatine transporter deficiency due to SLC6A8 mutation

American Journal of Medical Genetics, Part A
Myriam Abdennadher
exaly  

Efficacy of creatine supplementation in a patient with epilepsy with SLC6A8 gene mutations

Epileptic Disorders
exaly