Publication Cover
Hemoglobin
international journal for hemoglobin research
Volume 24, 2000 - Issue 4
22
Views
2
CrossRef citations to date
0
Altmetric
Original Article

HB Watford [βl(NA1)VAL→GLY]: A new, Clinically Silent Hemoglobin Variant in Linkage with a new Neutral Mutation [CAP +36 (G→A)]

, , , , &
Pages 347-353 | Published online: 07 Jul 2009

References

  • Kamel K., El‐Najjar A., Webber B. B., Chen S. S., Wilson J. B., Kutlar A., Huisman T. H.J. Hb Doha or α2β2‘X‐N‐Met‐ l (N Al )Val→Glu’ a new β chain abnormal hemoglobin observed in a Qatari female. Biochim. Biophys. Acta 1985; 831: 257–260
  • Boissel J. P., Kasper T. J., Shah S. C., Malone J. I., Bunn H. F. Amino‐terminal processing of proteins: Hemoglobin South Florida, a variant with retention of initiator methionine and N α acetylation. Proc. Natl. Acad. Sci. USA. 1985; 82: 8448–8452
  • Ohba Y., Hattori Y., Sakata S., Yamashiro Y., Okayama N., Hirano T., Nakanishi T., Miyazaki A., Shimizu A. Hb Niigata ‘βl(NAI)Val→Leu’: the fifth variant with retention of the initiator methionine and partial acetylation. Hemoglobin 1997; 21: 179–186
  • Moo‐Penn W. F., Bechtel K. C., Schmidt R. M., Johnson M. H., Jue D. L., Schmidt D. E., Dunlap W. M., Opella S. J., Bonaventura J., Bonaventura C. Hemoglobin Raleigh (βl Valine Acetytalanine). Structural and functional characterization. Biochemistry 1977; 16: 4872–4879
  • Boissel J. P., Kasper T. J., Bum H. F. Cotranslational amino‐terminal processing of cytosolic proteins. Cell free expression of site‐directed mutants of human hemoglobin. J. Biol. Chem. 1988; 263: 8443–8449
  • Quiu C. ‐C., Kasten‐Jolly J., Abraham E. C. Human red cell acetyltransferase. Life Sci. 1988; 42: 2739–2748
  • Thein S. L., Hinton J. A simple and rapid method of direct sequencing using Dyna‐beads. Br. J. Haematol. 1991; 79: 113–115
  • Perutz M. F., Lehmann H. Molecular pathology of human haemoglobin. Nature 1968; 219: 902–909
  • Doyle M. L., Lew G., Young A. D., Kwiatkowski L. D., Wierzba A. M., Noble R. W., Ackers G. K. Functional properties of human hemoglobins synthesized from recombinant mutant β‐globins. Biochemistry. 1992; 31: 8629–8639
  • Kister J., Préhu C., Riou J., Godart C., Bardakdjian J., Promé D., Galactéros F., Wajcman H. Two hemoglobin variants with an alteration of the oxygen‐linked chloride binding: Hb Antananarivo ‘β1(NAI)Val→Gly’ and Hb Barbizon ‘β144(HC1)Lys→Met’. Hemoglobin 1999; 23: 21–32
  • Ho P., Rochette J., Fisher C., Wonke B., Jarvis M., Yardumian A., Thein S. L. Moderate reduction of β globin gene transcript by a novel mutation in the 5′ untranslated region: a study of its interaction with other genotypes in two families. Blood 1996; 87: 1170–1178

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.