OPA1-related dominant optic atrophy is not strongly influenced by mitochondrial DNA background
OPA1-related dominant optic atrophy is not strongly influenced by mitochondrial DNA background
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Publisher
England: BioMed Central Ltd
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Language
English
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Publisher
England: BioMed Central Ltd
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Contents
Leber's hereditary optic neuropathy (LHON) and autosomal dominant optic atrophy (ADOA) are the most frequent forms of hereditary optic neuropathies. LHON is associated with mitochondrial DNA (mtDNA) mutations whereas ADOA is mainly due to mutations in the OPA1 gene that encodes a mitochondrial protein involved in the mitochondrial inner membrane re...
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Full title
OPA1-related dominant optic atrophy is not strongly influenced by mitochondrial DNA background
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TN_cdi_doaj_primary_oai_doaj_org_article_d57cb598c154427899524b9d0304ca4c
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_d57cb598c154427899524b9d0304ca4c
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ISSN
1471-2350,1471-2156
E-ISSN
1471-2350,1471-2156
DOI
10.1186/1471-2350-10-70
