Associated Papers
Structural model of the OPA1 GTPase domain may explain the molecular consequences of a novel mutation in a family with autosomal dominant optic atrophy.
Dadgar S et al.
Experimental Eye Research, 2006
OPA1 mutations and mitochondrial DNA haplotypes in autosomal dominant optic atrophy.
Han J et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2006
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