Stargardt disease
Description
Stargardt disease, also known as Stargardt 1 (STGD1), is an autosomal recessive form of retinal dystrophy that is usually characterized by a progressive loss of central vision associated with irregular macular and perimacular yellow-white fundus flecks, and a so-called ''beaten bronze'' atrophic central macular lesion.
Cell Lines
- LVPEIi007-B
- LVPEIi008-A
- LVPEIi008-B
- CUIMCi005-A
- ESi157-A
- ESi158-A
- FRIMOi003-A
- FRIMOi004-A
- IMOi001-A
- IMOi002-A
- IMOi003-A
- IMOi004-A
- IMOi005-A
- IMOi006-A
- RMCGENi005-A
- RMCGENi005-A-1
- RMCGENi005-A-1
- RMCGENi020-A
- RMCGENi021-A
- SCTCi017-A-1
- SCTCi018-A-1
- SCTi003-A-3
- SCTCi017-A
- SCTCi017-A-1
- SCTCi018-A
- SCTCi018-A-1