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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Bibliographic Details
Published in:Brain Pathol
Main Authors: Sase, Sunetra, Takanohashi, Asako, Vanderver, Adeline, Almad, Akshata
Format: Artigo
Language:Inglês
Published: John Wiley and Sons Inc. 2018
Subjects:
Mini‐symposium: Leukodystrophies Due to Astroyctic Dysfunction
Online Access: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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