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)
Etiology
germline nuclear gene mutations
See also
mitochondrial diseases
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