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November 1, 1994American Journal of Hematology

Compound heterozygosity for two α‐globin gene defects, Hb taybe (α1; 38 or 39 minus thr) and a poly a mutation (α2; AATAAA → AATAAG), results in a severe hemolytic anemia

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Authors

DPD. D. PobedimskayaInternational Science and Technology CenterTMT. P. MolchanovaLomonosov Moscow State UniversitySSSara Streichman

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Cite This Study

Pobedimskaya et al. (1994) studied this question.

synapsesocial.com/papers/6a943d2b1e998d99dafef83chttps://doi.org/10.1002/ajh.2830470310
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Hb H Disease Caused by a Homozygosity for the AATAAA→ AATAAG Mutation in the Polyadenylation Site of the α2-Globin Gene: Hematological Observations2009 · 33 citations
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  3. 3Hemoglobin Petah Tikva (alpha 110 ala replaced by asp): a new unstable variant with alpha-thalassemia-like expression1981 · 55 citations
  4. 4Construction of Human Gene Libraries from Small Amounts cf Peripheral Blood: Analysis of β-Like Globin Genes1982 · 568 citations
  5. 5A New Genetic Basis for Hemoglobin-H Disease1980 · 98 citations