A Rare Case of Epileptic Encephalopathy Caused by X-Linked <i>ALG13</i> Gene Mutation in a 6-Year-Old Girl

Authors

Hee Won Chueh (ORCID: https://orcid.org/0000-0002-3824-2334)
Kyung Ran Jun (ORCID: https://orcid.org/0000-0001-8904-2327)
Yun Jung Hur (ORCID: https://orcid.org/0000-0002-7633-925X)

Institutions

Inje University Haeundae Paik Hospital (KR)

Publication Details

Journal: Annals of Child Neurology
Published: 2025-06-25
DOI: https://doi.org/10.26815/acn.2024.00794
Primary Topic: Genetics and Neurodevelopmental Disorders
Type: article
Field-Weighted Citation Impact: 0.00

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article

A Rare Case of Epileptic Encephalopathy Caused by X-Linked ALG13 Gene Mutation in a 6-Year-Old Girl

Hee Won Chueh, Kyung Ran Jun, Yun Jung Hur

Jun 25, 2025

Annals of Child Neurology

Genetics and Neurodevelopmental Disorders

article

A Rare Case of Epileptic Encephalopathy Caused by X-Linked ALG13 Gene Mutation in a 6-Year-Old Girl

Hee Won Chueh, Kyung Ran Jun, Yun Jung Hur

June 25, 2025article en

Abstract

No abstract available for this paper.

Annals of Child Neurology

Inje University Haeundae Paik Hospital (KR)

Gender equality

Openalex Percentile: Top 83%

Genetics and Neurodevelopmental Disorders

DOI Open Access PDF OpenAlex

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A Rare Case of Epileptic Encephalopathy Caused by X-Linked <i>ALG13</i> Gene Mutation in a 6-Year-Old Girl — Hee Won Chueh, Kyung Ran Jun, et al. · Annals of Child Neurology (2025) | TGRS Research Map | TGRS