Increased risk of sensorineural hearing loss and migraine in patients with a rare mitochondrial DNA variant 4336A>G in tRNAGln

J Med Genet. 2001 Jun;38(6):400-5. doi: 10.1136/jmg.38.6.400.
No abstract available

Publication types

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

MeSH terms

  • Adenosine Triphosphatases / genetics
  • Adult
  • Aged
  • Animals
  • Cohort Studies
  • Conserved Sequence
  • DNA, Mitochondrial / genetics*
  • Evolution, Molecular
  • Female
  • Genetic Predisposition to Disease
  • Hearing Loss, Sensorineural / diagnosis
  • Hearing Loss, Sensorineural / genetics*
  • Humans
  • Male
  • Middle Aged
  • Migraine Disorders / diagnosis
  • Migraine Disorders / genetics*
  • Mitochondrial Proton-Translocating ATPases
  • Phylogeny
  • Polymorphism, Single Nucleotide*
  • RNA, Transfer, Gln / genetics*

Substances

  • DNA, Mitochondrial
  • MT-ATP6 protein, human
  • RNA, Transfer, Gln
  • Adenosine Triphosphatases
  • Mitochondrial Proton-Translocating ATPases