Infantile-onset deafness in m.7445A>G carriers may be multicausal

Int J Pediatr Otorhinolaryngol. 2018 Aug;111:192-193. doi: 10.1016/j.ijporl.2018.06.024. Epub 2018 Jun 14.
No abstract available

Publication types

  • Letter
  • Comment

MeSH terms

  • DNA, Mitochondrial
  • Deafness*
  • Heterozygote*
  • Humans
  • Mutation

Substances

  • DNA, Mitochondrial