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Optic Atrophy, Autosomal Dominant

"Optic Atrophy, Autosomal Dominant" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

Dominant optic atrophy is a hereditary optic neuropathy causing decreased visual acuity, color vision deficits, a centrocecal scotoma, and optic nerve pallor (Hum. Genet. 1998; 102: 79-86). Mutations leading to this condition have been mapped to the OPA1 gene at chromosome 3q28-q29. OPA1 codes for a dynamin-related GTPase that localizes to mitochondria.


This graph shows the total number of publications written about "Optic Atrophy, Autosomal Dominant" by people in Harvard Catalyst Profiles by year, and whether "Optic Atrophy, Autosomal Dominant" was a major or minor topic of these publication.
Bar chart showing 6 publications over 5 distinct years, with a maximum of 2 publications in 2017
To see the data from this visualization as text, click here.
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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.