Cone photoreceptor abnormalities correlate with vision loss in patients with Stargardt disease.

No abstract is available for this paper.

• Publication year

  2011

• Venue

  Investigative Ophthalmology and Visual Science

• Publication date

  2011-05-17

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1167/iovs.10-6538PMID 21296825PMCID PMC3109028
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Compléments : Fundus autofluorescence in stargardt macular dystrophy–fundus flavimaculatus

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• Age-related Macular Degeneration THE LIPOFUSCIN COMPONENT N-RETINYL-N-RETINYLIDENE ETHANOLAMINE DETACHES PROAPOPTOTIC PROTEINS FROM MITOCHONDRIA AND INDUCES APOPTOSIS IN MAMMALIAN RETINAL PIGMENT EPITHELIAL CELLS *

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• Corrigendum: A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy

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