Is X-linked, infantile onset ALG13-related developmental and epileptic encephalopathy a congenital disorder of glycosylation?

Epilepsia. 2021 Feb;62(2):335-336. doi: 10.1111/epi.16817. Epub 2021 Feb 11.
No abstract available

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Comment

MeSH terms

  • Glycosylation
  • Humans
  • N-Acetylglucosaminyltransferases
  • Spasms, Infantile* / genetics

Substances

  • ALG13 protein, human
  • N-Acetylglucosaminyltransferases