|
?:definition
|
-
Molecular assay reagents intended to identify deletions and duplications in genes associated with mitochondrial anemia, forms of hereditary anemia whose underlying cause is a deficit in mitochondrial function. Genetic variants at multiple loci have been associated with mitochondrial anemia. These reagents are intended to detect deletions and duplications in multiple mitochondrial anemia-associated loci simultaneously.
|
![[This page as RDF]](https://research.tib.eu/covid-19/static/rdf-icon.gif){kind=icon}