Mitochondrial DNA mutation 14487T>C manifesting as Leber’s hereditary optic neuropathy View Full Text


Ontology type: schema:ScholarlyArticle     

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s00415-015-7955-5

DOI

http://dx.doi.org/10.1007/s00415-015-7955-5

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1011434659

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/26530508


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