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Article

Genome sequencing identifies a non-coding variant in the MCDR1 locus as a cause of macular dystrophy.

Clinical & experimental ophthalmology - 1 Apr 2017

Ellingford Jamie M, Sergouniotis Panagiotis I, Jenkins Emma, Black Graeme C

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Share to Chromosome Mapping
Share to Corneal Dystrophies, Hereditary
Share to Eye Proteins
Share to Genetic Linkage

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genome, Human

Share to RNA, Untranslated

Share to Tomography, Optical Coherence

Share to Visual Acuity

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Identifiers

PMID: 27551809
DOI: 10.1111/ceo.12825

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