OPA3 gene

Known as: MGA3, FLJ22187, OPA3 
 

Topic mentions per year

Topic mentions per year

2001-2017
02420012017

Papers overview

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2012
2012
atrophy and nystagmus since the first year of life, (2) progressive loss of vision, and (3) bilateral cerulean cataract at age 37… (More)
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2011
2011
PURPOSE Autosomal-dominant optic atrophy (DOA) is one of the most common inherited optic neuropathies, and it is genetically… (More)
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2010
2010
3-Methylglutaconic aciduria type III (3-MGCA type III), caused by recessive mutations in the 2-exon gene OPA3, is characterized… (More)
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2010
2010
Costeff Syndrome, which is caused by mutations in the OPTIC ATROPHY 3 (OPA3) gene, is an early-onset syndrome characterized by… (More)
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2008
2008
Opa3 mRNA is expressed in all tissues examined to date, but currently the function of the OPA3 protein is unknown. Intriguingly… (More)
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2006
2006
Autosomal dominant optic atrophy (ADOA) is genetically heterogeneous, with OPA1 on 3q28 being the most prevalently mutated gene… (More)
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2005
2005
We have screened 13 patients with neurological abnormalities and 3-methylglutaconic aciduria (3MGA) for mutations in the OPA3… (More)
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2004
2004
H ereditary optic atrophy is a generic term that refers to a heterogeneous group of genetic disorders for which several modes of… (More)
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2002
2002
Type III 3-methylglutaconic aciduria (MGA) (MIM 258501) consists of early bilateral optic atrophy, later development of… (More)
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Highly Cited
2001
Highly Cited
2001
Type III 3-methylglutaconic aciduria (MGA) (MIM 258501) is a neuro-ophthalmologic syndrome that consists of early-onset bilateral… (More)
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