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

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

Research output: Contribution to journal › Comment/debate

4 Scopus citations

Original language	English
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
Externally published	Yes

Access to Document

10.1111/epi.16817

Cite this

@article{916696e2225f483b9308045924d7af41,

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",

year = "2021",

month = feb,

doi = "10.1111/epi.16817",

language = "English",

volume = "62",

pages = "335--336",

journal = "Epilepsia",

issn = "0013-9580",

publisher = "Wiley-Blackwell Publishing Ltd",

number = "2",

}

TY - JOUR

T1 - Is X-linked, infantile onset ALG13-related developmental and epileptic encephalopathy a congenital disorder of glycosylation?

AU - Berry, Gerard T.

AU - Freeze, Hudson H.

AU - Morava, Eva

PY - 2021/2

Y1 - 2021/2

UR - https://www.scopus.com/pages/publications/85101236990

U2 - 10.1111/epi.16817

DO - 10.1111/epi.16817

M3 - Comment/debate

C2 - 33576051

AN - SCOPUS:85101236990

SN - 0013-9580

VL - 62

SP - 335

EP - 336

JO - Epilepsia

JF - Epilepsia

IS - 2

ER -