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CONE DYSTROPHY, X-LINKED, 1

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

Related topics

Related topics

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
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… 
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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