GNAT2 gene

Known as: G PROTEIN, ALPHA-TRANSDUCING 2, G protein subunit alpha transducin 2, TRANSDUCIN, CONE-SPECIFIC, ALPHA POLYPEPTIDE 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1988-2018
024619882018

Papers overview

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2014
2014
PURPOSE To characterize retinal structure and function in achromatopsia (ACHM) in preparation for clinical trials of gene therapy… (More)
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Highly Cited
2013
Highly Cited
2013
Approaches exploiting trait distribution extremes may be used to identify loci associated with common traits, but it is unknown… (More)
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2006
2006
PURPOSE To report a novel mouse model of achromatopsia with a cpfl3 mutation found in the ALS/LtJ strain. METHODS The effects… (More)
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Highly Cited
2005
Highly Cited
2005
Achromatopsia is a congenital, autosomal recessively inherited disorder characterized by a lack of color discrimination, low… (More)
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2005
2005
Unrelated patients with achromatopsia, macular degeneration with onset under age 50 years, cone degeneration or dysfunction, cone… (More)
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2004
2004
PURPOSE The present study was designed to elucidate the molecular genetic basis of a congenital stationary cone dysfunction… (More)
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2004
2004
C omplete achromatopsia or rod monochromatism is a stationary cone dystrophy, with an incidence of ,1 in 30 000, in which… (More)
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2003
2003
AIM To describe the phenotype of a three generation consanguineous Pakistani family containing six individuals with autosomal… (More)
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Highly Cited
2002
Highly Cited
2002
Achromatopsia is an autosomal recessively inherited visual disorder that is present from birth and that features the absence of… (More)
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2002
2002
OBJECTIVE To determine the molecular basis for achromatopsia using autozygosity mapping and positional candidate gene analysis… (More)
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