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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

176 related items for PubMed ID: 10400133

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  • 6. Two novel HADHB gene mutations in a Korean patient with mitochondrial trifunctional protein deficiency.
    Park HD, Kim SR, Ki CS, Lee SY, Chang YS, Jin DK, Park WS.
    Ann Clin Lab Sci; 2009; 39(4):399-404. PubMed ID: 19880769
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  • 14. Identification of a Novel HADHB Gene Mutation in an Iranian Patient with Mitochondrial Trifunctional Protein Deficiency.
    Shahrokhi M, Shafiei M, Galehdari H, Shariati G.
    Arch Iran Med; 2017 Jan; 20(1):22-27. PubMed ID: 28112527
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  • 16. Two alpha subunit donor splice site mutations cause human trifunctional protein deficiency.
    Brackett JC, Sims HF, Rinaldo P, Shapiro S, Powell CK, Bennett MJ, Strauss AW.
    J Clin Invest; 1995 May; 95(5):2076-82. PubMed ID: 7738175
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  • 17. A fetal fatty-acid oxidation disorder as a cause of liver disease in pregnant women.
    Ibdah JA, Bennett MJ, Rinaldo P, Zhao Y, Gibson B, Sims HF, Strauss AW.
    N Engl J Med; 1999 Jun 03; 340(22):1723-31. PubMed ID: 10352164
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  • 18. Molecular and phenotypic heterogeneity in mitochondrial trifunctional protein deficiency due to beta-subunit mutations.
    Spiekerkoetter U, Sun B, Khuchua Z, Bennett MJ, Strauss AW.
    Hum Mutat; 2003 Jun 03; 21(6):598-607. PubMed ID: 12754706
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