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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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| Pubblicato in: | Brain Pathol |
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| Autori principali: | , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
John Wiley and Sons Inc.
2018
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| Soggetti: | |
| Accesso online: | 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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