Literature DB >> 1670860

Mitochondrial leucine tRNA mutation in a mitochondrial encephalomyopathy.

H Ino, M Tanaka, K Ohno, K Hattori, S Ikebe, T Sano, T Ozawa, T Ichiki, M Kobayashi, Y Wada.   

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Year:  1991        PMID： 1670860     DOI： 10.1016/0140-6736(91)92196-9

Source DB:  PubMed          Journal:  Lancet        ISSN： 0140-6736            Impact factor:   79.321


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  3 in total

1.  Multiple enzyme defects in mitochondria of a case with congenital lactic acidosis and hyperammonaemia.

Authors:  M Kobayashi; T Ichiki; N Sugiyama; T Sano; K Ban; T Tsuboi; H Inagaki; K Okajima; H Sobajima; S Suzuki
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

2.  Epilepsy in a mitochondrial disorder.

Authors:  T Torbergsen; E Mathiesen; J Aasly
Journal:  J Neurol Neurosurg Psychiatry       Date:  1991-12       Impact factor: 10.154

Review 3.  Nucleus-driven mutations of human mitochondrial DNA.

Authors:  M Zeviani
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982
  3 in total

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