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CONE DYSTROPHY, X-LINKED, 1

Known as: COD1, CONE DYSTROPHY 1, X-LINKED 
National Institutes of Health

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3 relations
CONE-ROD DYSTROPHY, X-LINKED, 1

Broader (2)

Genetic Diseases, X-LinkedRetinitis Pigmentosa

Papers overview

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2011
2011
Searching For Meaningful Use Of Health Information Technology A Study Of Cardiovascular Disease Care In Veterans General Hospitals
2003
2003
A new genetic locus for X linked progressive cone-rod dystrophy
X linked progressive cone-rod dystrophy (COD) is a retinal disease primarily affecting the cone photoreceptors. The disease is… 
2003
2003
Refinement of the Physical Location and the Genomic Characterization of the CRSP2 (EXLM1) Gene on Xp11.4
In the course of our search for the gene responsible for X-linked cone-rod dystrophy (COD1), we constructed a physical map and… 
2001
2001
Identification, genomic structure, and screening of the vacuolar proton-ATPase membrane sector-associated protein M8-9 gene within the COD1 critical region (Xp11.4).
PURPOSE Our goal is to identify the gene responsible for X-linked cone-rod dystrophy (COD1) that has been localized to a limited… 
Highly Cited
2000
Highly Cited
2000
Remapping of the RP15 locus for X-linked cone-rod degeneration to Xp11.4-p21.1, and identification of a de novo insertion in the RPGR exon ORF15.
X-linked forms of retinitis pigmentosa (XLRP) are among the most severe, because of their early onset, often leading to… 
1998
1998
Linkage analysis of X-linked cone-rod dystrophy: localization to Xp11.4 and definition of a locus distinct from RP2 and RP3.
Progressive X-linked cone-rod dystrophy (COD1) is a retinal disease affecting primarily the cone photoreceptors. The COD1 locus… 
1994
1994
Clinical diversity and chromosomal localization of X-linked cone dystrophy (COD1).
X-linked progressive cone dystrophy (COD1) causes progressive deterioration of visual acuity, deepening of central scotomas… 
1994
1994
Refined localization of an X-linked cone-rod dystrophy (COD1)
Several of us previously reported linkage of a COD1 family to DXS7 and MAOA, assigned to Xp11.3. Two recombination events between… 
1993
1993
Additional evidence for a gene locus for progressive cone dystrophy with late rod involvement in Xp21.1-p11.3.
X-linked progressive cone dystrophy (XLPCD) is a rare hereditary eye disorder characterized by disturbed cone ERG, abnormal color… 
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