Compound Heterozygosity for Hb Tacoma [β30(B12)Arg→Ser] and β+-Thalassemia
Author:
Publisher
Informa UK Limited
Subject
Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630260008997534
Reference17 articles.
1. New unstable haemoglobin (Hb Moscva, β24 (B4) Gly→Asp) found in the USSR
2. An unstable haemoglobin, Hb Tacoma beta30 (B12) arg leads to ser, detected at birth by the demonstration of red cell inclusions.
3. Rare β Chain Hemoglobin Variants Found in Swedish Patients During HBA1cAnalysis
4. Two new sickle cell syndromes: HbS, Hb Camden, and alpha-thalassemia; and HbS in combination with Hb Tacoma
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1. The prevalence of hemoglobin Tacoma in Finland detected by HbA1c capillary electrophoresis;Scandinavian Journal of Clinical and Laboratory Investigation;2023-01-12
2. Unstable abnormal hemoglobins found in Russia in the past 10 years;Pediatric Hematology/Oncology and Immunopathology;2022-10-10
3. A novel means of identifying hemoglobin Tacoma utilizing capillary electrophoresis with a hemoglobin A1c software platform;Cogent Medicine;2021-01-01
4. A Novel Mutation at HBB: c.91delA (Codon 30, –A) Causing β-Thalassemia in a Chinese Family;Acta Haematologica;2019
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