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Leber's hereditary optic neuropathy: implications of the sex ratio for linkage studies in families with the 3460 ND1 mutation.

作者信息

Black G C, Craig I W, Oostra R J, Norby S, Rosenberg T, Morten K, Laborde A, Poulton J

机构信息

Department of Biochemistry, University of Oxford, UK.

出版信息

Eye (Lond). 1995;9 ( Pt 4):513-6. doi: 10.1038/eye.1995.117.

Abstract

Leber's hereditary optic neuropathy (LHON), which is associated with mutations in mitochondrial DNA (mtDNA), is commoner in males than females. A study of over 30 LHON families with a mutation at position 3460 of mtDNA demonstrates a significantly decreased male excess from that generally quoted, with evidence for a marked bias in the ascertainment of males over females. This has implications for the analysis of those factors which give rise to the male bias.

摘要

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