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January 1, 1997Hemoglobin

α-Thalassemia Caused by a 16 BP Deletion in the 3′ Untranslated Region of the α2-Globin Gene Including the First Nucleotide of the Poly a Signal Sequence

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Authors

HTHannah TamaryTel Aviv UniversityGKGil KlingerTel Aviv UniversityLSLea ShalmonRabin Medical Center

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Tamary et al. (1997) studied this question.

synapsesocial.com/papers/6a6fa9b8e5469ee92be08993https://doi.org/10.3109/03630269708997516
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Also Consider

Synapse has enriched 4 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1A new deletional α‐thalassemia detected in yemenites with hemoglobin H disease1994 · 17 citations
  2. 2Detection and Characterization of a 3′ Untranslated Region Ribonucleoprotein Complex Associated with Human α-Globin mRNA Stability1995 · 196 citations
  3. 3The 3′ noncoding region of β-globin mRNA is not essential for in vitro translation1979 · 43 citations
  4. 4The poly(A)-poly(A)-binding protein complex is a major determinant of mRNA stability in vitro.1989 · 378 citations