Predominantly Cone-System Dysfunction as Rare Form of Retinal Degeneration in Patients With Molecularly Confirmed Bardet-Biedl Syndrome. [electronic resource]
Producer: 20150928Description: 364-372.e1 p. digitalISSN:- 1879-1891
- Adult
- Bardet-Biedl Syndrome -- complications
- DNA -- genetics
- DNA Mutational Analysis
- Electroretinography
- Eye Proteins -- genetics
- Female
- Fluorescein Angiography
- Fundus Oculi
- Humans
- Male
- Middle Aged
- Mutation
- Phenotype
- Retinal Cone Photoreceptor Cells -- physiology
- Retinal Degeneration -- etiology
- Retrospective Studies
- Tomography, Optical Coherence
- Visual Acuity
- Visual Fields
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Publication Type: Journal Article; Multicenter Study; Observational Study; Research Support, Non-U.S. Gov't
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