Kinetics of Heterogeneous Background in Stargardt’s Disease over Time
Stargardt’s disease (STGD1) is caused by mutations in the <i>ABCA4</i> gene. Different lesions characterised by decreased autofluorescence levels are found in fundus autofluorescence (FAF) from STGD1 patients and could be used as outcome indicators for disease progression. We investigate...
Main Authors: | , , , , , |
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Format: | Article |
Language: | English |
Published: |
MDPI AG
2022-03-01
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Series: | Life |
Subjects: | |
Online Access: | https://www.mdpi.com/2075-1729/12/3/381 |