MELAS syndrome with mitochondrial tRNA(Leu(UUR)) gene mutation in a Chinese family.

Benzer Materyaller

• Pancreatic exocrine dysfunction associated with mitochondrial tRNA(Leu)(UUR) mutation.
  Yazar:: Onishi, H, ve diğerleri
  Baskı/Yayın Bilgisi: (1998)
• Heterogeneous presentation in A3243G mutation in the mitochondrial tRNA(Leu(UUR)) gene
  Yazar:: Koga, Y., ve diğerleri
  Baskı/Yayın Bilgisi: (2000)
• The mitochondrial tRNA(Leu(UUR)) mutation in mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes (MELAS): genetic, biochemical, and morphological correlations in skeletal muscle.
  Yazar:: Moraes, C T, ve diğerleri
  Baskı/Yayın Bilgisi: (1992)
• Nephropathy and growth hormone deficiency in a patient with mitochondrial tRNA(Leu(UUR)) mutation.
  Yazar:: Yorifuji, T, ve diğerleri
  Baskı/Yayın Bilgisi: (1996)
• Respiration-deficient cells are caused by a single point mutation in the mitochondrial tRNA-Leu (UUR) gene in mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS).
  Yazar:: Kobayashi, Y, ve diğerleri
  Baskı/Yayın Bilgisi: (1991)