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Hemoglobin
international journal for hemoglobin research
Volume 16, 1992 - Issue 1-2
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Original Article

A New α Chain Variant, HB Turriff [α99(66)LYS→6LU]: The Interference of Abnormal Hemoglobins in HB A1C Detemination

J. V. Langdorm Department of Haematology, Addenbrooke's Hospital, Hills Road, Cambridge, CB2 2QQ, UK
,
R. J. L. Davidson Department of Haematology, Aberdeen Royal Infirmary, Foresterhill, Aberdeen, AB9 2ZB, UK
&
D. Williamson University, Department of Haematology, MRC Centre Hills Road, Cambridge, CB2 2QH, UK
Pages 11-17 | Received 23 Jul 1991, Accepted 27 Nov 1991, Published online: 07 Jul 2009

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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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Nooshin Bayat, Samaneh Farashi, Nima Hafezi-Nejad, Negin Faramarzi, Mehri Ashki, Shadi Vakili, Hashem Imanian, Mohsen Khosravi, Azita Azar-Keivan & Hossein Najmabadi. (2013) Novel Mutations Responsible for α-Thalassemia in Iranian Families. Hemoglobin 37:2, pages 148-159.
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M. F. H. Carver & T. H. J. Huisman. (1997) International Hemoglobin Information Center Variant List. Hemoglobin 21:6, pages 505-506.
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. (1996) Variants of the Alpha Chain. Hemoglobin 20:3, pages 215-312.
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. (1994) International Hemoglobin Information Center. Hemoglobin 18:2, pages 77-161.
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. (1993) Variants of the Alpea Chain. Hemoglobin 17:2, pages 89-177.
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Articles from other publishers (11)

Neha Yadav & Amit Kumar Mandal. (2022) Interference of hemoglobin variants in HbA1c quantification. Clinica Chimica Acta.
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CF Chen & YK Tai. (2014) A rare haemoglobin variant (Hb Phnom Penh) manifesting as a falsely high haemoglobin A1c value on ion-exchange chromatography. Singapore Medical Journal 55:8, pages e126-e128.
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Chunjiang Zhu, Wenfang Yu, Jiansheng Xie, Ling Chen, Hui Ding, Xuan Shang & Xiangmin Xu. (2010) Hemoglobin H disease due to a de novo mutation at the α2-globin gene and an inherited common α-thalassemia deletion found in a Chinese boy. Blood Cells, Molecules, and Diseases 45:3, pages 223-226.
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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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Wolfgang J. Schnedl, Andrea Liebminger, Regina E. Roller, Rainer W. Lipp & Guenter J. Krejs. (2001) Hemoglobin variants and determination of glycated hemoglobin (HbA1c). Diabetes/Metabolism Research and Reviews 17:2, pages 94-98.
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Lynn Bry, Philip C Chen & David B Sacks. (2001) Effects of Hemoglobin Variants and Chemically Modified Derivatives on Assays for Glycohemoglobin. Clinical Chemistry 47:2, pages 153-163.
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William L Roberts, Elizabeth L Frank, Linda Moulton, Christine Papadea, Jimmie K Noffsinger & Ching-Nan Ou. (2000) Effects of Nine Hemoglobin Variants on Five Glycohemoglobin Methods. Clinical Chemistry 46:4, pages 560-576.
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Tsuyoshi Watanabe, Ken Kato, Daishiro Yamada, Sanae Midorikawa, Wakano Sato, Masaru Shiga, Yoshihiko Otsuka, Masakazu Miura, Keiko Harano & Teruo Harano. (1998) A Nondiabetic Case of Hemoglobin Variant (Hb Niigata) with Inappropriately High and Low HbA1c Titers Detected by Different Methods. Clinical Chemistry 44:7, pages 1562-1564.
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Shiu Chuen Wong & Tar Choon Aw. (1998) Hb E1c as an Indicator for the Presence of Hb AE Phenotype in Diabetic Patients. Clinical Chemistry 44:3, pages 660-662.
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W. J. Schnedl, E. C. Reisinger, R. W. Lipp, P. Hopmeier & G. J. Krejs. (1995) Hemoglobin variants recently detected in Austria. Annals of Hematology 71:4, pages 185-187.
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