Controller-gene diseases: The operon model as applied to β-thalassemia, familial fetal hemoglobinemia and the normal switch from the production of fetal hemoglobin to that of adult hemoglobin
- 1 January 1964
- journal article
- research article
- Published by Elsevier in Journal of Molecular Biology
- Vol. 8 (1), 128-147
- https://doi.org/10.1016/s0022-2836(64)80154-6
Abstract
No abstract availableKeywords
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