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CACNA1F gene

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

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Highly Cited
2009
Highly Cited
2009
Zebra chip (ZC), an emerging disease causing economic losses to the potato chip industry, has been reported since the early 1990s… Expand
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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… Expand
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Highly Cited
2006
Highly Cited
2006
Glutamate release from photoreceptor terminals is controlled by voltage-dependent calcium channels (VDCCs). In humans, mutations… Expand
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Highly Cited
2006
Highly Cited
2006
Background: X linked cone-rod dystrophy (CORDX) is a recessive retinal disease characterised by progressive dysfunction of… Expand
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Highly Cited
2005
Highly Cited
2005
Retinal neural transmission represents a key function of the eye. Identifying the molecular components of this vital process is… Expand
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Highly Cited
2005
Highly Cited
2005
Light stimuli produce graded hyperpolarizations of the photoreceptor plasma membrane and an associated decrease in a voltagegated… Expand
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Highly Cited
2005
Highly Cited
2005
Objective: To assess the rate of cartilage loss, the change in bone marrow edema pattern and internal joint derangement at 1.5-T… Expand
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2002
2002
X-linked CSNB patients may exhibit myopia, nystagmus, strabismus and ERG abnormalities of the Schubert-Bornschein type. We… Expand
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Highly Cited
2001
Highly Cited
2001
Abstract. Incomplete X-linked congenital stationary night blindness (CSNB) is a recessive, non-progressive eye disorder… Expand
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Highly Cited
2000
Highly Cited
2000
BACKGROUND Incomplete X-linked congenital stationary night blindness (CSNB) is a clinically variable condition that has been… Expand
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