Co-inheritance of heterozygous 0-thalassemia with single functional -globin gene: challenges of carrier detection in pre-marital screening program for thalassemia

HIGHLIGHTS

• who: Hossein Jalali et al. from the Research Center, Hemoglobinopathies Institute, Mazandaran University of Medical Sciences, Sari, Iran have published the paper: Co-Inheritance of Heterozygous 0-Thalassemia with Single Functional -Globin Gene: Challenges of Carrier Detection in Pre-Marital Screening Program for Thalassemia, in the Journal: (JOURNAL)
• what: This study aimed to report on the co-inheritance of α- and β-thalassemia mutations in a female case with normal HbA2 levels, while her wife was a β-thalassemia carrier.
• how: The results indicated that the male and(Sebia femaleFrance) subjects were β and amp α-thalassemia capillary . . .
  

   

  

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