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  • Molecular assay reagents intended to identify genetic variants associated with Leber hereditary optic neuropathy, a mitochondrial disorder associated with a range of symptoms including vision and hearing loss. Genetic variants at multiple loci have been associated with Leber hereditary optic neuropathy. These reagents are intended to detect various types of genetic changes (e.g., deletions, duplications, insertions, single nucleotide polymorphisms) in multiple Leber hereditary optic neuropathy-associated loci simultaneously.
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