Evaluation of Local Rod and Cone Function in Stargardt Disease

Author:

Stingl Krunoslav12,Hoyng Carel3,Kempf Melanie12,Kohl Susanne4,Jung Ronja1,Righetti Giulia1,Kühlewein Laura14,Pohl Lisa1,Kortüm Friederike1,Kelbsch Carina15,Wilhelm Barbara56,Peters Tobias456,Stingl Katarina12,

Affiliation:

1. University Eye Hospital, Center for Ophthalmology, University of Tuebingen, Tuebingen, Germany

2. Center for Rare Eye Diseases, University of Tuebingen, Tuebingen, Germany

3. Department of Ophthalmology, Radboud University Medical Centre, 6500HB Nijmegen, the Netherlands

4. Institute for Ophthalmic Research, Center for Ophthalmology, University of Tuebingen, Tuebingen, Germany

5. Pupil research group, University of Tuebingen, Tuebingen, Germany

6. STZ eyetrial at the Center for Ophthalmology, University Tuebingen, Tuebingen, Germany

Publisher

Association for Research in Vision and Ophthalmology (ARVO)

Subject

General Medicine

Reference33 articles.

1. A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy;Allikmets;Nat Genet,1997

2. Peripheral pigmented retinal lesions in Stargardt disease;Zhao;Am J Ophthalmol,2018

3. Fundus flavimaculatus. Clinical, functional and histopathologic observations;Klien;Am J Ophthalmol,1967

4. Variation of clinical expression in patients with Stargardt dystrophy and sequence variations in the ABCR gene;Fishman;Arch Ophthalmol,1999

5. Alterations of slow and fast rod ERG signals in patients with molecularly confirmed Stargardt disease type 1;Scholl;Invest Ophthalmol Vis Sci,2002

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