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March 1, 1988Journal of Biological ChemistryOpen Access

Dysfunctional alpha-globin gene in hemoglobin H disease in blacks. A dinucleotide deletion produces a frameshift and a termination codon.

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Authors

SSSurinder SafayaKing Faisal UniversityRRRonald F. RiederState University of New York

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Safaya et al. (1988) studied this question.

synapsesocial.com/papers/6a6fa9b8e5469ee92be08997https://doi.org/10.1016/s0021-9258(18)68929-x
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Also Consider

Synapse has enriched 3 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1A new gene deletion in the alpha-like globin gene cluster as the molecular basis for the rare alpha-thalassemia-1(--/alpha alpha) in blacks: HbH disease in sickle cell trait.1986 · 30 citations
  2. 2Initiation codon mutation as a cause of alpha thalassemia.1984 · 129 citations
  3. 3Proportion of hemoglobin G Philadelphia (alpha 268 Asn leads to Lys beta 2) in heterozygotes is determined by alpha-globin gene deletions.1980 · 37 citations