The spectrum of beta-thalassemia mutations in the 22 Arab countries: a systematic review.
CONCLUSION: The findings of this study present a platform for further genetic epidemiological studies and will improve the genetic counseling for Arab patients with β-thal.
PMID: 33317346 [PubMed - as supplied by publisher]
Source: Expert Review of Hematology - Category: Hematology Tags: Expert Rev Hematol Source Type: research
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