Clinical utility of whole genome sequencing for the detection of mitochondrial genome mutations

J Genet Genomics. 2020 Mar 20;47(3):167-169. doi: 10.1016/j.jgg.2020.03.001. Epub 2020 Mar 19.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • DNA, Mitochondrial / genetics
  • Genetic Diseases, Inborn / diagnosis*
  • Genetic Diseases, Inborn / genetics
  • Genetic Predisposition to Disease*
  • Genome, Mitochondrial / genetics*
  • Humans
  • Mutation / genetics
  • Whole Genome Sequencing*

Substances

  • DNA, Mitochondrial