Defects in mitochondrial protein synthesis and respiratory chain activity segregate with the tRNA (Leu (UUR)) mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes

• KING M. P.

収録刊行物

• Mol. Cell. Biol.

  Mol. Cell. Biol. 12 480-490, 1992

詳細情報

• CRID: 1570009751775544448
• NII論文ID: 80006298017
• データソース種別:
  • CiNii Articles