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GNAT2 gene

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

Papers overview

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2016
2016
PurposeThe 2 most common causative genes for achromatopsia (ACHM) are CNGA3 and CNGB3; other genes including GNAT2 account for… Expand
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2013
2013
Abstract Transducin is a heterotrimeric G protein that plays a critical role in phototransduction in the rod and cone… Expand
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2011
2011
Complete achromatopsia is a rare autosomal recessive disease associated with CNGA3, CNGB3, GNAT2 and PDE6C mutations. This… Expand
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2009
2009
We studied a polygenic region located on Chromosome (Chr) lq in Chinese hamster cells that is coamplified along with the AMPD2… Expand
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Highly Cited
2006
Highly Cited
2006
PURPOSE To report a novel mouse model of achromatopsia with a cpfl3 mutation found in the ALS/LtJ strain. METHODS The effects… Expand
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1998
1998
PURPOSE The alpha-subunit of human cone transducin plays an important role in interacting with visual pigment and activating the… Expand
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1995
1995
We report localization of the human cone transducin (GNAT2) gene using fluorescence in situ hybridization on chromosome 1 in band… Expand
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1995
1995
Stargardt's disease is an autosomal recessive infantile macular degeneration of unknown origin whose gene has been recently… Expand
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1995
1995
Stargardt's disease is an autosomal recessive infantile macular degeneration of unknown origin whose gene has been recently… Expand
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1988
1988
A variety of genes have been identified that specify the synthesis of the components of guanine nucleotide-binding proteins (G… Expand
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