Literature DB >> 2030983

A polymorphic synonymous mutation in human ornithine-delta-aminotransferase (N378N).

L S Martin1, G A Mitchell, J Michaud, L C Brody, D Valle.   

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Year:  1991        PMID： 2030983      PMCID： PMC328151          DOI： 10.1093/nar/19.8.1962

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN： 0305-1048            Impact factor:   16.971


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  3 in total

1.  Human ornithine-delta-aminotransferase. cDNA cloning and analysis of the structural gene.

Authors:  G A Mitchell; J E Looney; L C Brody; G Steel; M Suchanek; J F Engelhardt; H F Willard; D Valle
Journal:  J Biol Chem       Date:  1988-10-05       Impact factor: 5.157

2.  Investigation of gyrate atrophy using a cDNA clone for human ornithine aminotransferase.

Authors:  V Ramesh; M M Shaffer; J M Allaire; V E Shih; J F Gusella
Journal:  DNA       Date:  1986-12

3.  Molecular cloning of human ornithine aminotransferase mRNA.

Authors:  G Inana; S Totsuka; M Redmond; T Dougherty; J Nagle; T Shiono; T Ohura; E Kominami; N Katunuma
Journal:  Proc Natl Acad Sci U S A       Date:  1986-03       Impact factor: 11.205
  3 in total
  1 in total

1.  Pyridoxine-responsive gyrate atrophy of the choroid and retina: clinical and biochemical correlates of the mutation A226V.

Authors:  J Michaud; G N Thompson; L C Brody; G Steel; C Obie; G Fontaine; K Schappert; C G Keith; D Valle; G A Mitchell
Journal:  Am J Hum Genet       Date:  1995-03       Impact factor: 11.025
  1 in total

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