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Nucleic Acids Res. 1986 March 11; 14(5): 2408.
PMCID: PMC339667

Antithrombin III tours gene: identification of a point mutation leading to an arginine----cysteine replacement in a silent deficiency.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.
  • Chasse JF, Esnard F, Guitton JD, Mouray H, Perigois F, Fauconneau G, Gauthier F. An abnormal plasma antithrombin with no apparent affinity for heparin. Thromb Res. 1984 May 15;34(4):297–302. [PubMed]
  • Huynh-Dinh T, Duchange N, Zakin MM, Lemarchand A, Igolen J. Modified oligonucleotides as alternatives to the synthesis of mixed probes for the screening of cDNA libraries. Proc Natl Acad Sci U S A. 1985 Nov;82(22):7510–7514. [PubMed]
  • Prochownik EV, Markham AF, Orkin SH. Isolation of a cDNA clone for human antithrombin III. J Biol Chem. 1983 Jul 10;258(13):8389–8394. [PubMed]
  • Koide T, Odani S, Takahashi K, Ono T, Sakuragawa N. Antithrombin III Toyama: replacement of arginine-47 by cysteine in hereditary abnormal antithrombin III that lacks heparin-binding ability. Proc Natl Acad Sci U S A. 1984 Jan;81(2):289–293. [PubMed]
  • Sakuragawa N, Takahashi K, Kondo S, Koide T. Antithrombin III Toyama: a hereditary abnormal antithrombin III of a patient with recurrent thrombophlebitis. Thromb Res. 1983 Jul 15;31(2):305–317. [PubMed]

Articles from Nucleic Acids Research are provided here courtesy of Oxford University Press