Updates on Emerging Interventions for Autosomal Recessive ABCA4-Associated Stargardt Disease

Autosomal recessive Stargardt disease (STGD1) is an inherited retinal degenerative disease associated with a mutated ATP-binding cassette, subfamily A, member 4 (ABCA4) gene. STGD1 is the most common form of juvenile macular degeneration with onset in late childhood to early or middle adulthood and...

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Detalles Bibliográficos
Autores principales: Wang, Liang, Shah, Serena M., Mangwani-Mordani, Simran, Gregori, Ninel Z.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10573680/
https://www.ncbi.nlm.nih.gov/pubmed/37834872
http://dx.doi.org/10.3390/jcm12196229

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10573680/
https://www.ncbi.nlm.nih.gov/pubmed/37834872
http://dx.doi.org/10.3390/jcm12196229

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