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mitochondrial traduction anomalies

Etiology

- germline nuclear gene mutations

  • MRPS16
  • MRPS22
  • EFG1
  • TSFM
  • TUFM
  • TRMU
  • RARS2
  • DARS2
  • C12Orf65
  • PUS1
  • YARS2
  • SARS2
  • HARS2

See also

- mitochondrial diseases

  • respiratory chain deficiency (OXPHOS system deficiency)