2003-03-01
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
Publication
Publication
Hemoglobin: international journal for hemoglobin research , Volume 27 - Issue 1 p. 49- 51
Additional Metadata | |
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doi.org/10.1081/HEM-120018437, hdl.handle.net/1765/53788 | |
Hemoglobin: international journal for hemoglobin research | |
Organisation | Department of Hematology |
Harteveld, C., van Lom, K., Gómez García, E., van Delft, P., & Giordano, P. C. (2003). 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. Hemoglobin: international journal for hemoglobin research, 27(1), 49–51. doi:10.1081/HEM-120018437 |