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January 1, 1982Nucleic Acids ResearchOpen Access

Duplication followed by deletion accounts for the structure of an Indian deletion βo-thalassemia gene

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Authors

RSRichard A. SpritzRegeneron (United States)Stuart H. OrkinStuart H. OrkinBroad Institute

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Spritz et al. (1982) studied this question.

synapsesocial.com/papers/6a9b1e8e0beea8855ec61afehttps://doi.org/10.1093/nar/10.24.8025
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Also Consider

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

  1. 1Five nucleotide changes in the large intervening sequence of a β globin gene in a β+thalassemia patient1982 · 31 citations
  2. 2beta-Thalassemia in a Kurdish Jew. Single base changes in the T-A-T-A box.1982 · 105 citations
  3. 3A nucleotide change at a splice junction in the human beta-globin gene is associated with beta 0-thalassemia.1981 · 103 citations
  4. 4Structure and expression of a cloned β°thalassaemic globin gene1981 · 85 citations
  5. 5Analysis of Globin Gene Structure in Patients with β Thalassemia by Restriction Endonuclease Mapping1981 · 5 citations