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Astrocytes, an active player in Aicardi–Goutières syndrome

Aicardi–Goutières syndrome (AGS) is an early‐onset, autoimmune and genetically heterogeneous disorder with severe neurologic injury. Molecular studies have established that autosomal recessive mutations in one of the following genes are causative: TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR1 a...

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Shranjeno v:
Bibliografske podrobnosti
izdano v:Brain Pathol
Main Authors: Sase, Sunetra, Takanohashi, Asako, Vanderver, Adeline, Almad, Akshata
Format: Artigo
Jezik:Inglês
Izdano: John Wiley and Sons Inc. 2018
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC8028286/
https://ncbi.nlm.nih.gov/pubmed/29740948
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/bpa.12600
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