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CONE-ROD DYSTROPHY, X-LINKED, 1

Known as: CORDX1, Cone-Rod Dystrophy, X-Linked, Type 1 
National Institutes of Health

Related topics

Related topics

4 relations
CONE DYSTROPHY, X-LINKED, 1RPGR gene

Broader (2)

Genetic Diseases, X-LinkedRetinitis Pigmentosa

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2008
2008
Molecular genetics of X-linked cone-rod dystrophy and Åland Island eye disease
X-linked cone-rod dystrophy is a retinal disease characterized by progressive loss of cone and rod photoreceptor functions… 
2005
2005
Histopathologic study of X- linked cone- rod dystrophy (CORDX1) caused by a mutation in the RPGR exon ORF15
Purpose: To evaluate the donor retina of a patient with X- linked cone- rod dystrophy caused by an RPGR exon ORF15 mutation… 
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