Aicardi-Goutières syndrome type 7 in a Chinese child: A case report

BACKGROUND: IFIH1 is a protein-coding gene. Disorders associated with IFIH1 include Aicardi-Goutières syndrome (AGS) type 7 and Singleton-Merten syndrome type 1. Related pathways include RIG-I/MDA5-mediated induction of the interferon (IFN)-α/β pathway and the innate immune system. AGS type 7 is an...

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Detalles Bibliográficos
Autores principales: Lin, Shuang-Zhu, Yang, Jing-Jing, Xie, Tian-Long, Li, Jia-Yi, Ma, Jia-Qi, Wu, Si, Wang, Na, Wang, Yong-Ji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10130998/
https://www.ncbi.nlm.nih.gov/pubmed/37123312
http://dx.doi.org/10.12998/wjcc.v11.i11.2452

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10130998/
https://www.ncbi.nlm.nih.gov/pubmed/37123312
http://dx.doi.org/10.12998/wjcc.v11.i11.2452

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