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- W2252744481 abstract "A new beta(0) thalassemia allele caused by a TGAT insert in codon 116 of exon III was detected in a patient compound heterozygous for beta(0) thalassemia / Hb D Los Angeles and his father. The mutation unexpectedly causes a classical thalassemic phenotype. The compound heterozygosity leads to mild microcytic anemia and no further clinical signs." @default.
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- W2252744481 date "2005-11-01" @default.
- W2252744481 modified "2023-09-23" @default.
- W2252744481 title "A 4 base pair TGAT insertion at codon 116 of the beta globin gene causes beta0-thalassemia." @default.
- W2252744481 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/16266911" @default.
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