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Stargardt disease: Multimodal imaging: A review

Stargardt disease (STGD1) is an autosomal recessive retinal dystrophy, characterised by bilateral progressive central vision loss and subretinal deposition of lipofuscin‐like substances. Recent advances in molecular diagnosis and therapeutic options are complemented by the increasing recognition of...

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Detalles Bibliográficos
Autores principales:	Heath Jeffery, Rachael C., Chen, Fred K.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley & Sons Australia, Ltd 2021
Materias:	Reviews
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8366508/ https://www.ncbi.nlm.nih.gov/pubmed/34013643 http://dx.doi.org/10.1111/ceo.13947

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