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Hb Rambam [beta69(E13)Gly-->Asp]/beta0-thalassemia [codon 5 (-CT)] in a family from Argentina.

AuthorsD Plaseska-Karanfilska, B I de Weinstein, G D Efremov
JournalHemoglobin (Hemoglobin) Vol. 24 Issue 2 Pg. 157-61 (May 2000) ISSN: 0363-0269 [Print] England
PMID10870889 (Publication Type: Case Reports, Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Hemoglobins
  • Hemoglobins, Abnormal
  • hemoglobin Rambam
Topics
  • Anemia (blood, genetics)
  • Argentina
  • Blood Cells (pathology)
  • Child
  • Chromatography, High Pressure Liquid
  • DNA Mutational Analysis
  • Electrophoresis
  • Erythrocyte Indices
  • Family Health
  • Fathers
  • Frameshift Mutation
  • Hematologic Tests
  • Hemoglobins (analysis, metabolism)
  • Hemoglobins, Abnormal (chemistry, genetics)
  • Humans
  • Italy (ethnology)
  • Male
  • Point Mutation
  • beta-Thalassemia (genetics)

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