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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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Detalles Bibliográficos
Autores principales:	Jabri, Yassin, Biber, Josef, Diaz-Lezama, Nundehui, Grosche, Antje, Pauly, Diana
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2020
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7697683/ https://www.ncbi.nlm.nih.gov/pubmed/33187113 http://dx.doi.org/10.3390/ijms21228468

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