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

HB Nottingum or α2β298(F65)VAL→GLY Observed as a De Novo Mutation in a Canadian Child

B. Cepreganova Laboratory of Protein Chemistry Department of Biochemistry and Molecular Biology, Medical College of Georgia, Augusta, GA, 30912-2100, USA
,
J. B. Wilson Laboratory of Protein Chemistry Department of Biochemistry and Molecular Biology, Medical College of Georgia, Augusta, GA, 30912-2100, USA
,
T. H. J. Huisman Laboratory of Protein Chemistry Department of Biochemistry and Molecular Biology, Medical College of Georgia, Augusta, GA, 30912-2100, USA
&
H. A. Hume Department of Pediatrics, Hopital Sainte-Justine, Montreal, Quebec, Canada, H3T 1C5
Pages 77-79 | Received 10 Sep 1991, Accepted 22 Nov 1991, Published online: 07 Jul 2009

Citations (7)

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Read on this site (3)

Rong-Yue Wang, Fan Jiang, Li-Li Xu & Dong-Zhi Li. (2021) Mild α-Thalassemia Caused by a Mosaic α-Globin Gene Mutation. Hemoglobin 45:2, pages 140-141.
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Yuko Cho, Susumu Iizuka, Yoshio Hatae, Kunihiko Kobayashi, Yukio Hattori, Yasuhiro Yamashiro & Tadashi Ariga. (2012) A 25-Year Observation of a Japanese Female Patient with Hb Nottingham who has Two Children with the Same Disorder. Hemoglobin 36:5, pages 446-455.
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Giuseppina Lacerra, Rosario Testa, Maria De Angioletti, Gino Schilirò & Clementina Carestia. (2003) Hb Bronte or α93(FG5)Val→Gly: A New Unstable Variant of the α2‐Globin Gene, Associated with a Mild α+‐Thalassemia Phenotype. Hemoglobin 27:3, pages 149-159.
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Articles from other publishers (4)

Aisyah Aziz, Mohd Farid Baharin, Muhammad Yusri Fauzi, Faidatul Syazlin Abdul Hamid, Thiyagar Nadarajaw, Rahimah Ahmad & Hafizah Hashim. (2022) Rare cause of transfusion‐dependent hemolytic anemia: A case report of HbE/Hb Nottingham and literature review. Pediatric Blood & Cancer 69:9.
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Stavros G. Memtsoudis, Robert W. LekowskiJRJR, Peter Rosenberger, Zain Khalpey, Daniel J. FitzGerald, Valorie Claypoole, Kevin D. Courtney, Michael J. Landzberg, H. Franklin Bunn & Prem S. Shekar. (2016) Pulmonary thrombectomy in a patient with hemoglobin Nottingham. Perfusion 22:4, pages 299-301.
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V. Brabec, K. Indrák, H. Fořtová, J. Suttnar, B. Blažek, J. Čermák, V. Divoký, L. Vepřeková & J. Zeman. (1994) Hb Nottingham or α2β2 98 (FG5) Val→Gly in a Czech child. Annals of Hematology 69:2, pages 93-95.
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Britta Landin, Björn Fröstad, Mats Brune & Rolf Ljung. (2009) Haemoglobin Köln as de novo mutations in Sweden: Diagnosis by PCR and specific enzymatic cleavage . European Journal of Haematology 52:3, pages 156-161.
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