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The Dutch IVS-I-116 (A --> G) (alpha2) thalassemia mutation induces Hb H inclusion bodies when found in combination with the -alpha3.7 deletion defect
Authors:Harteveld Cornelis L  Van Lom Kirsten  Gomez Garcia Encarna B  van Delft Peter  Giordano Piero C
Affiliation:Hemoglobinopathies Laboratory, Department of Human and Clinical Genetics, Leiden University Medical Center, AL Leiden, The Netherlands.
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