Novel non-contiguous exon duplication in choroideremia
T L Edwards1,2, J Williams3, M I Patrício1
1Department of Clinical Neurosciences, Nuffield Laboratory of Ophthalmology, University of Oxford, Oxford, UK.
Clinical Genetics
|April 4, 2017
Summary
Establishing a genetic diagnosis for choroideremia is crucial with new gene therapies. This study found complex DNA duplications in a patient, potentially creating abnormal proteins affecting photoreceptors and gene therapy outcomes.
Area of Science:
- Genetics
- Ophthalmology
- Molecular Biology
Background:
- Choroideremia is an X-linked inherited retinal disease causing progressive vision loss.
- Genetic diagnosis is vital for patients, especially with emerging gene replacement therapies.
- The CHM gene provides instructions for making Rab escort protein 1 (REP-1).
Keywords:
choroideremiacopy number variationgenetic testingophthalmologyretinal dystrophystructural variationMore Related Videos
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