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A novel mutation (LEU396ARG) in OPA1 is associated with a severe phenotype in a large dominant optic atrophy pedigree
M J Schnieders1,2, W Goar2,3, M Griess3
1Department of Biochemistry, Carver College of Medicine, University of Iowa, Iowa, IA, USA.
Eye (London, England)
|January 20, 2018
Abstract
No abstract available in PubMed .
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