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Hemoglobin
international journal for hemoglobin research
Volume 26, 2002 - Issue 3
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FOUR NEW β CHAIN HEMOGLOBIN VARIANTS WITHOUT CLINICAL OR HEMATOLOGICAL EFFECTS: Hb SAN BRUNO [β39(C5)Gln→His]; Hb FORT DODGE [β93(F9)Cys→Tyr]; Hb RHODE ISLAND [β116(G18)His→Tyr]; AND Hb INGLEWOOD [β142(H20)Ala→Thr]

James D. Hoyer Department of Laboratory Medicine and Pathology, Mayo Clinic, 200 First Street, Rochester, MN 55905, USA
,
Daniel J. McCormick Department of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, MN, 55905, USA
,
Karen Snow Department of Laboratory Medicine and Pathology, Mayo Clinic, 200 First Street, Rochester, MN 55905, USA
,
Kathleen S. Kubik Department of Laboratory Medicine and Pathology, Mayo Clinic, 200 First Street, Rochester, MN 55905, USA
,
Michael W. Holmes Department of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, MN, 55905, USA
,
D. Brian Dawson Department of Laboratory Medicine and Pathology, Mayo Clinic, 200 First Street, Rochester, MN 55905, USA
,
Ruth Shaber Department of Obstetrics and Gynecology, Kaiser-Permanente Foundation of South San Francisco, South San Francisco, CA 94080, USA
,
Mark Marner Associated Internists, P.C., Fort Dodge, IA 50501, USA
,
Jennifer Hosmer The Providence Community Health Centers, Inc., Providence, RI 02908, USA
,
Nancy Shinno Kaiser-Permanente Foundation of Southern California, Inglewood, CA 90301, USA
&
Virgil F. Fairbanks Department of Laboratory Medicine and Pathology, Mayo Clinic, 200 First Street, Rochester, MN 55905, USA
 show all
Pages 299-303 | Received 25 Apr 2002, Accepted 16 May 2002, Published online: 07 Jul 2009

REFERENCES

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  • Krishnan K., Martinez F., Wille R. T., Jones R. T., Shih D. T., Head C., Fairbanks V. F., Dabich L. Hb Washtenaw [β11(A8)Val→Phe] an Electrophoretically Silent, Unstable, Low Oxygen Affinity Variant Associated with Anemia and Chronic Cyanosis. Hemoglobin 1994; 8 (4&5): 285–295
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  • Kendall A. G., ten Pas A., Wilson J. B., Cope N., Bolch K., Huisman T.H. J. Hb Vaasa or α2β2 [39(C5)Gln→Glu], a Mildly Unstable Variant Found in a Finnish Family. Hemoglobin 1977; 1(2)292–295
  • Li H-J., Zhao X-N., Li H-W., Li L., Liang K-X., Wang R-P., Chang T-T., Wilson J. B., Webber B. B., Huisman T.H. J. A New Slow-Moving Hemoglobin Variant Hb Tianshui or α2β2 39(C5)Gln→Arg, Observed in a Chinese Family Living in Gansu. Hemoglobin 1990; 14(5)569–570
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  • Blanke S., Johnsen A., Wimberley P. D., Mortensen H. B. Hemoglobin Hafnia: α2(β116 (G18) His→Gln)2; a New Hemoglobin Variant Mistaken for Glycated Hemoglobin. Biochim. Biophys. Acta 1988; 955(2)214–219
  • Moo-Penn W. F., Schneider R. G., Shih T-B., Jones R. T., Govindarajan S., Govindarajan P. G., Patchen L. C. Hemoglobin Ohio (β142 Ala→Asp): a New Abnormal Hemoglobin with High Oxygen Affinity and Erythrocytosis. Blood 1980; 56(2)246–250
  • Imai K., Yoshioka Y., Tyuma I., Hirano M. Functional Abnormalities of Hemoglobin Toyoake (142 (H20)β, Ala→Pro). Biochim. Biophys. Acta 1981; 668(1)1–15
  • Hirano M., Ohba Y., Imai K., Ino T., Morishita Y., Matsui T., Shimizu S., Sumi H., Yamamoto K., Miyaji T. Hb Toyoake: β142 (H20) Ala→Pro. a New Unstable Hemoglobin with High Oxygen Affinity. Blood 1981; 59(4)697–704

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