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Spectral-domain optical coherence tomography findings in Alström syndrome
BACKGROUND: Alström syndrome is a multi-system recessive disorder caused by mutations in ALMS1 gene. The aim of this study was to characterize morphological retinal changes in Alström patients using spectral-domain optical coherence tomography. METHODS: We studied volunteer patients attending the co...
Shranjeno v:
| izdano v: | Ophthalmic Genet |
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| Main Authors: | , , , , , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
2017
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5557692/ https://ncbi.nlm.nih.gov/pubmed/28112973 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1080/13816810.2016.1257029 |
| Oznake: |
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