Evidence against an X-linked locus close to DXS7 determining visual loss susceptibility in British and Italian families with Leber hereditary optic neuropathy.

Leber hereditary optic neuropathy (LHON) is associated with mutations of mtDNA, but two features of LHON pedigrees are not explicable solely on the basis of mitochondrial inheritance. There is a large excess of affected males, and not all males at risk develop the disease. These observations could b...

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Bibliografiske detaljer
Main Authors: Sweeney, M G, Davis, M B, Lashwood, A, Brockington, M, Toscano, A, Harding, A E
Format: Artigo
Sprog:Inglês
Udgivet: 1992
Fag:
Research Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1682819/
https://ncbi.nlm.nih.gov/pubmed/1415219
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