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Journal Abstract Search


147 related items for PubMed ID: 8634714

  • 1. Partial characterization and assignment of the gene for protoporphyrinogen oxidase and variegate porphyria to human chromosome 1q23.
    Roberts AG, Whatley SD, Daniels J, Holmans P, Fenton I, Owen MJ, Thompson P, Long C, Elder GH.
    Hum Mol Genet; 1995 Dec; 4(12):2387-90. PubMed ID: 8634714
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  • 5. Molecular basis of variegate porphyria: a missense mutation in the protoporphyrinogen oxidase gene.
    Frank J, Lam H, Zaider E, Poh-Fitzpatrick M, Christiano AM.
    J Med Genet; 1998 Mar; 35(3):244-7. PubMed ID: 9541112
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  • 10. Expression and characterization of six mutations in the protoporphyrinogen oxidase gene among Finnish variegate porphyria patients.
    von und zu Fraunberg M, Tenhunen R, Kauppinen R.
    Mol Med; 2001 May; 7(5):320-8. PubMed ID: 11474578
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  • 12. Recurrent missense mutation in the protoporphyrinogen oxidase gene underlies variegate porphyria.
    Frank J, Jugert FK, Breitkopf C, Goerz G, Merk HF, Christiano AM.
    Am J Med Genet; 1998 Aug 27; 79(1):22-6. PubMed ID: 9738863
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  • 17. Lack of the R59W South African founder effect mutation in protoporphyrinogen oxidase in a British patient with homozygous variegate porphyria.
    McGrath JA, Hawk JL, Graham RM, Christiano AM.
    Br J Dermatol; 1997 Feb 27; 136(2):292. PubMed ID: 9068758
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  • 19. Nine novel mutations in the protoporphyrinogen oxidase gene in Swedish families with variegate porphyria.
    Wiman A, Harper P, Floderus Y.
    Clin Genet; 2003 Aug 27; 64(2):122-30. PubMed ID: 12859407
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