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

Gerard T. Berry; Hudson H. Freeze; Eva Morava

doi:10.1111/epi.16817

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

Gerard T. Berry, Hudson H. Freeze, Eva Morava

Medical Genetics

Research output: Contribution to journal › Comment/debate › peer-review

1 Scopus citations

Original language	English (US)
Pages (from-to)	335-336
Number of pages	2
Journal	Epilepsia
Volume	62
Issue number	2
DOIs	https://doi.org/10.1111/epi.16817
State	Published - Feb 2021

ASJC Scopus subject areas

Neurology
Clinical Neurology

Access to Document

10.1111/epi.16817

Cite this

@article{842d22a3cfaa4db79f9cf92bafd22c34,

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

author = "Berry, {Gerard T.} and Freeze, {Hudson H.} and Eva Morava",

note = "Funding Information: Frontiers in Congenital Disorders of Glycosylation (1U54NS115198‐01) was funded by the National Institute of Neurological Diseases and Stroke and the National Center for Advancing Translational Sciences (G.T.B., H.H.F., and E.M.) and the Rocket Fund (H.H.F.). ",

year = "2021",

month = feb,

doi = "10.1111/epi.16817",

language = "English (US)",

volume = "62",

pages = "335--336",

journal = "Epilepsia",

issn = "0013-9580",