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Advances in Imaging of Stargardt Disease
Stargardt disease (STGD1) is an autosomal-recessively inherited condition often associated with mutations in ABCA4 and characterized by accumulation of autofluorescent lipofuscin deposits in the retinal pigment epithelium (RPE). Non-invasive imaging techniques including fundus autofluorescence (FAF)...
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| Publicado no: | Adv Exp Med Biol |
|---|---|
| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4862575/ https://ncbi.nlm.nih.gov/pubmed/20238033 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/978-1-4419-1399-9_38 |
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