Literature DB >> 14755384

Thalassemia beta0 due to an identical frameshift mutation, codon 15 (-T) in both parents.

Bani Gajra, Debasis Bandyopadhyay, Shila Chakrabarti, Bani Sengupta, Madhusnata De, R V Shaji, Geeta Talukder.   

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Year:  2004        PMID： 14755384     DOI： 10.1002/ajh.10461

Source DB:  PubMed          Journal:  Am J Hematol        ISSN： 0361-8609            Impact factor:   10.047


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  1 in total

1.  Thalassemia intermedia phenotype resulting from rare combination of c.46delT [Codon15 (-T)] mutation of beta globin gene and HPFH3.

Authors:  Anjali J Kelkar; Anu Moses
Journal:  Clin Case Rep       Date:  2017-05-26
  1 in total

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