Clinical and laboratory features of hemoglobin la desirade variant in association with sickle cell and alpha thalassemia genes

S. Alkindi*, S. Al Zadjali, M. Al Rawahi, H. Al Haddabi, S. Daar, R. A. ElSadek, B. D. Sherkawy, A. V. Pathare

*Corresponding author for this work

Research output: Contribution to journalLetterpeer-review

1 Citation (Scopus)
Original languageEnglish
Article numbere2021010
JournalMediterranean Journal of Hematology and Infectious Diseases
Issue number1
Publication statusPublished - Jan 2021


  • Alpha thalassemia
  • Hemoglobin La Desirade
  • Sickle cell disease
  • Sickle cell trait
  • Unstable hemoglobin variant

ASJC Scopus subject areas

  • Hematology
  • Infectious Diseases

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