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Hemoglobin
international journal for hemoglobin research
Volume 26, 2002 - Issue 2
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FOUR NEW VARIANTS OF THE α2-GLOBIN GENE WITHOUT CLINICAL OR HEMATOLOGIC EFFECTS: Hb PARK RIDGE [α9(A7)Asn→Lys (α2)], Hb NORTON [α72(EF1)His→Asp (α2)], HbLOMBARD [α103(G10)His→Tyr (α2)], AND Hb SAN ANTONIO [α113(GH2)Leu→Arg (α2)]

James D. Hoyer Department of Laboratory Medicine and Pathology, Mayo Clinic, 200 First Street, Rochester, MN, 55905, U.S.A.
,
Daniel J. McCormick Department of Biochemistry and Molecular Biology, Mayo Clinic, 200 First Street, Rochester, MN, 55905, U.S.A.
,
Karen Snow Department of Laboratory Medicine and Pathology, Mayo Clinic, 200 First Street, Rochester, MN, 55905, U.S.A.
,
Jong H. Kwon Lutheran General Children's Hospital, Park Ridge, IL, 60068, U.S.A.
,
David Booth Norton Family Practice Clinic, Muskegon Heights, MI, 49444, U.S.A.
,
Manuel Duarte National University of Health Science, Lombard, IL, 60148, U.S.A.
,
Guy Grayson Pediatric Hematology and Oncology Associates of South Texas, San Antonio, TX, 78229, U.S.A.
,
Kathleen S. Kubik Department of Laboratory Medicine and Pathology, Mayo Clinic, 200 First Street, Rochester, MN, 55905, U.S.A.
,
Michael W. Holmes Department of Biochemistry and Molecular Biology, Mayo Clinic, 200 First Street, Rochester, MN, 55905, U.S.A.
&
Virgil F. Fairbanks Department of Laboratory Medicine and Pathology, Mayo Clinic, 200 First Street, Rochester, MN, 55905, U.S.A.
 show all
Pages 175-180 | Received 26 Dec 2001, Published online: 07 Jul 2009

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Read on this site (2)

Agathe Horri-Naceur & David J. Timson. (2020) In Silico Analysis of the Effects of Point Mutations on α-Globin: Implications for α-Thalassemia. Hemoglobin 44:2, pages 89-103.
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Cornelis L. Harteveld, Peter Van Delft, Robert J. Plug, Zoran Erjavec, Henri Wajcman & Piero C. Giordano. (2002) Hb DELFZICHT [α9(A7)Asn→Lys (α1)]: A NEW, CLINICALLY SILENT HEMOGLOBIN VARIANT OBSERVED IN A DUTCH PATIENT. Hemoglobin 26:2, pages 181-184.
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Articles from other publishers (3)

Kaavya Krishna Kumar, David A. Jacques, J. Mitchell Guss & David A. Gell. (2014) The structure of α-haemoglobin in complex with a haemoglobin-binding domain from Staphylococcus aureus reveals the elusive α-haemoglobin dimerization interface . Acta Crystallographica Section F Structural Biology Communications 70:8, pages 1032-1037.
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Xiang YuTodd L. MollanAndrew Butler, Andrew J. Gow, John S. OlsonMitchell J. Weiss. (2009) Analysis of human α globin gene mutations that impair binding to the α hemoglobin stabilizing protein. Blood 113:23, pages 5961-5969.
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Corinne Vasseur-Godbillon, Michael C. Marden, Piero Giordano, Henri Wajcman & Véronique Baudin-Creuza. (2006) Impaired binding of AHSP to α chain variants: Hb Groene Hart illustrates a mechanism leading to unstable hemoglobins with α thalassemic like syndrome. Blood Cells, Molecules, and Diseases 37:3, pages 173-179.
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