The Dutch IVS‐I‐116 (A→G) (α2) Thalassemia Mutation Induces Hb H Inclusion Bodies When Found in Combination with the −α^3.7 Deletion Defect

Cornelis L. Harteveld Hemoglobinopathies Laboratory, Department of Human and Clinical Genetics, Leiden University Medical Center, Wassenaarseweg 72, 2333, AL Leiden, The Netherlands

Kirsten Van Lom Department of Hematology, Erasmus Medical Center, GD Rotterdam, The Netherlands

Encarna B. Gomez Garcia Department of Hematology, Erasmus Medical Center, GD Rotterdam, The Netherlands

Peter van Delft Hemoglobinopathies Laboratory, Department of Human and Clinical Genetics, Leiden University Medical Center, Wassenaarseweg 72, 2333, AL Leiden, The Netherlands

Piero C. Giordano Hemoglobinopathies Laboratory, Department of Human and Clinical Genetics, Leiden University Medical Center, Wassenaarseweg 72, 2333, AL Leiden, The Netherlands

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Xiao-Hong He, Rui Zhang, Guang-Xing Mai, Li-Rong Ren & Dong-Zhi Li. (2018) First Report of a Case with Nondeletional Hb H Disease Caused by IVS-I-116 (A>G) of the α2-Globin Gene. Hemoglobin 42:5-6, pages 344-346.
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Articles from other publishers (1)

Paul Dainer, Niren Patel, Lina Zhuang, Harris Carmichael & Ferdane Kutlar. (2014) Nondeletional ?-Thalassemia (?2- IVS-1-116, A>G HBA2): An ?2 Gene Point Mutation Detected in an African-American Female for the First Time. Acta Haematologica 132:1, pages 22-23.
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The Dutch IVS‐I‐116 (A→G) (α2) Thalassemia Mutation Induces Hb H Inclusion Bodies When Found in Combination with the −α^3.7 Deletion Defect

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The Dutch IVS‐I‐116 (A→G) (α2) Thalassemia Mutation Induces Hb H Inclusion Bodies When Found in Combination with the −α3.7 Deletion Defect

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The Dutch IVS‐I‐116 (A→G) (α2) Thalassemia Mutation Induces Hb H Inclusion Bodies When Found in Combination with the −α^3.7 Deletion Defect