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[In a Brazilian populaiton with beta Thalassemia, the beta 0 codon 39 nonsense mutation was the most frequent alteration (50.9%), followed by beta+ IVSI 110 G > A (18.1%), beta 0 IVSI 1 G > A (12.9%), beta+ IVSI 6 T > C (9.5%), and other rare mutations (8.6%]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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Gene-disease associations inferred from text-mining the literature.
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