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CACNA1F gene

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

Related topics

Related topics

3 relations
CONE DYSTROPHY 4 (disorder)CONE-ROD DYSTROPHY, X-LINKED, 3NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A

Papers overview

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Highly Cited
2018
Highly Cited
2018
The Synergistic Effects of Orthokeratology and Atropine in Slowing the Progression of Myopia
Atropine and orthokeratology (OK) are both effective in slowing the progression of myopia. In the current study, we studied the… 
2011
2011
Effect of irradiation times on the polymerization depth of contemporary fissure sealants with different opacities.
The aim of this study was to evaluate the depth of curing of 10 contemporary blue light-activated dental flowable materials at… 
Highly Cited
2009
Highly Cited
2009
First Report of the Detection of 'Candidatus Liberibacter' Species in Zebra Chip Disease-Infected Potato Plants in the United States.
Zebra chip (ZC), an emerging disease causing economic losses to the potato chip industry, has been reported since the early 1990s… 
Highly Cited
2007
Highly Cited
2007
A novel CACNA1F gene mutation causes Aland Island eye disease.
PURPOSE Aland Island eye disease (AIED), also known as Forsius-Eriksson syndrome, is an X-linked recessive retinal disease… 
2005
2005
Novel mutations in CACNA1F and NYX in Dutch families with X-linked congenital stationary night blindness.
PURPOSE To describe the clinical features and genetic analysis of eight X-linked congenital stationary night blindness (XLCSNB… 
Highly Cited
2005
Highly Cited
2005
Clinical manifestations of a unique X‐linked retinal disorder in a large New Zealand family with a novel mutation in CACNA1F, the gene responsible for CSNB2
Purpose: To describe the phenotype in a New Zealand family with an unusual severe X‐linked retinal disorder with a novel I745T… 
2003
2003
Mutations in the CACNA1F and NYX genes in British CSNBX families
X‐linked congenital stationary night blindness (CSNBX) is a genetically and phenotypically heterogeneous non‐progressive disorder… 
2003
2003
Retinal and optic disc atrophy associated with a CACNA1F mutation in a Japanese family.
OBJECTIVE To describe retinal and optic disc atrophy and a progressive decrease of visual function in 2 Japanese brothers. Both… 
Highly Cited
2002
Highly Cited
2002
Thirty distinct CACNA1F mutations in 33 families with incomplete type of XLCSNB and Cacna1f expression profiling in mouse retina
X-linked CSNB patients may exhibit myopia, nystagmus, strabismus and ERG abnormalities of the Schubert-Bornschein type. We… 
Highly Cited
2001
Highly Cited
2001
A summary of 20 CACNA1F mutations identified in 36 families with incomplete X-linked congenital stationary night blindness, and characterization of splice variants
Abstract. Incomplete X-linked congenital stationary night blindness (CSNB) is a recessive, non-progressive eye disorder… 
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