top of page

[New paper] SLC35A2 mutation in intractable epilepsy

A new paper published in Neurology Genetics.

In this study, Hyeonju Son and Sangwoo Kim analyzed sequencing data from patients with intractable epilepsy to confirm that mutations in SLC35A2 is the cause of the epilepsy with aberrant N-glycosylation.

"Brain somatic mutations in SLC35A2 cause intractable epilepsy with aberrant N-glycosylation", Neurology Genetics 2018, 4:e294

Featured Posts
Recent Posts
Search By Tags
Follow Us
  • Facebook Basic Square
  • Twitter Basic Square
  • Google+ Basic Square
bottom of page