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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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| Publicat a: | Brain Pathol |
|---|---|
| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
John Wiley and Sons Inc.
2018
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| Matèries: | |
| Accés en línia: | 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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