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Article

Retinal microstructure in patients with EFEMP1 retinal dystrophy evaluated by Fourier domain OCT.

Eye (London, England) - 1 Feb 2009

Gerth C, Zawadzki R J, Werner J S, Héon E

Abstract excerpt

OBJECTIVES: To investigate retinal microstructure of patients affected with malattia leventinese (MLVT) and mutation in the EFEMP1 gene using high-resolution optical coherence tomography (OCT). METHODS: Patients diagnosed with MLVT received a comprehensive eye exam, full-field and multifocal electroretinogram testing and imaging with a high-resolution Fourier domain OCT (Fd-OCT, UC Davis Medical Center, Davis,...

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Share to Electroretinography
Share to Extracellular Matrix Proteins
Share to Eye Diseases, Hereditary

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Retinal Degeneration

Share to Retinal Pigment Epithelium

Share to Tomography, Optical Coherence

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Source

Open in PubMed Open full text

Identifiers

PMID: 18791549
DOI: 10.1038/eye.2008.251
PMCID: PMC2734481

Genes

RPE
EFEMP1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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