CACNA1F gene

Known as: OA2, CALCIUM CHANNEL, VOLTAGE-DEPENDENT, ALPHA-1F SUBUNIT, CACNA1F 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1990-2017
051019902017

Papers overview

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2007
2007
PURPOSE Aland Island eye disease (AIED), also known as Forsius-Eriksson syndrome, is an X-linked recessive retinal disease… (More)
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Highly Cited
2006
Highly Cited
2006
Mutations in genes encoding either components of the phototransduction cascade or proteins presumably involved in signaling from… (More)
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2005
2005
Objective: To assess the rate of cartilage loss, the change in bone marrow edema pattern and internal joint derangement at 1.5-T… (More)
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2005
2005
Light stimuli produce graded hyperpolarizations of the photoreceptor plasma membrane and an associated decrease in a voltagegated… (More)
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2005
2005
PURPOSE To describe the phenotype in a New Zealand family with an unusual severe X-linked retinal disorder with a novel I745T… (More)
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2004
2004
OBJECTIVE To use high-resolution magnetic resonance imaging (MRI) to determine the relationship between articular cartilage… (More)
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2002
2002
X-linked CSNB patients may exhibit myopia, nystagmus, strabismus and ERG abnormalities of the Schubert-Bornschein type. We… (More)
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2001
2001
Incomplete X-linked congenital stationary night blindness (CSNB) is a recessive, non-progressive eye disorder characterized by… (More)
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2000
2000
BACKGROUND Incomplete X-linked congenital stationary night blindness (CSNB) is a clinically variable condition that has been… (More)
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Highly Cited
1998
Highly Cited
1998
X-linked congenital stationary night blindness (CSNB) is a recessive non-progressive retinal disorder characterized by night… (More)
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