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Cell-Type-Specific Complement Profiling in the ABCA4(−/−) Mouse Model of Stargardt Disease
Stargardt macular degeneration is an inherited retinal disease caused by mutations in the ATP-binding cassette subfamily A member 4 (ABCA4) gene. Here, we characterized the complement expression profile in ABCA4(−/−) retinae and aligned these findings with morphological markers of retinal degenerati...
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| Pubblicato in: | Int J Mol Sci |
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| Autori principali: | , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
MDPI
2020
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7697683/ https://ncbi.nlm.nih.gov/pubmed/33187113 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms21228468 |
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