Validation of a MGM1/OPA1 chimeric gene for functional analysis in yeast of mutations associated with dominant optic atrophy
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Molecular Medicine
Reference62 articles.
1. OPA1, encoding a dynamin- related GTPase, is mutated in autosomal dominant optic atrophy linked to chromosome 3q28;Alexander;Nat. Genet.,2000
2. OPA1-associated disorders: phenotypes and pathophysiology;Amati-Bonneau;Int. J. Biochem. Cell Biol.,2009
3. The association of autosomal dominant optic atrophy and moderate deafness may be due to the R445H mutation in the OPA1 gene;Amati-Bonneau;Am J. Ophthalmol.,2003
4. OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes;Amati-Bonneau;Brain,2008
5. Saccharomyces cerevisiae;Ausubel;Curr. Protoc. Mol. Biol.,1994
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