Your search for "opa3" returned 115 TaqMan® SNP Genotyping Assays
optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)
The mouse ortholog of this protein co-purifies with the mitochondrial inner membrane. Mutations in this gene have been shown to result in 3-methylglutaconic aciduria type III and autosomal dominant optic atrophy and cataract. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2009]
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