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Deletion of the OPA1 gene in a dominant optic atrophy family: evidence that haploinsufficiency is the cause of disease
Authors:Marchbank N J  Craig J E  Leek J P  Toohey M  Churchill A J  Markham A F  Mackey D A  Toomes C  Inglehearn C F
Affiliation:Molecular Medicine Unit, University of Leeds, Clinical Sciences Building, St James's University Hospital, Leeds LS9 7TF, UK.
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