Literature DB >> 8098444

Japanese case of diabetes mellitus and deafness with mutation in mitochondrial tRNA(Leu(UUR)) gene.

T Awata, T Matsumoto, Y Iwamoto, A Matsuda, T Kuzuya, T Saito.   

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Year:  1993        PMID： 8098444     DOI： 10.1016/0140-6736(93)91204-y

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


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  5 in total

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Authors:  G Costi; S Ten; N K Maclaren
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Review 2.  Maternally inherited diabetes and deafness: a new diabetes subtype.

Authors:  J A Maassen; T Kadowaki
Journal:  Diabetologia       Date:  1996-04       Impact factor: 10.122

3.  Pancreatic beta-cell secretory defect associated with mitochondrial point mutation of the tRNA(LEU(UUR)) gene: a study in seven families with mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS).

Authors:  S Suzuki; Y Hinokio; S Hirai; M Onoda; M Matsumoto; M Ohtomo; H Kawasaki; Y Satoh; H Akai; K Abe
Journal:  Diabetologia       Date:  1994-08       Impact factor: 10.122

4.  Association of polymorphism in the interferon gamma gene with IDDM.

Authors:  T Awata; C Matsumoto; T Urakami; R Hagura; S Amemiya; Y Kanazawa
Journal:  Diabetologia       Date:  1994-11       Impact factor: 10.122

5.  Mitochondrial complex I and V gene polymorphisms in type II diabetes mellitus among high risk Mizo-Mongoloid population, Northeast India.

Authors:  Freda Lalrohlui; Sunaina Thapa; Souvik Ghatak; John Zohmingthanga; Nachimuthu Senthil Kumar
Journal:  Genes Environ       Date:  2016-03-01
  5 in total

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