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Editorial office, Journal of Blood Disorder and Treatment, United Kingdom

Publications

  • Opinion   
    Sickle cell anaemia
    Author(s): Tom Bells*

    Chain generation in thalassemia is lacking or decreased as a result of molecular abnormalities. Because the synthesis of the alpha chain is unaffected, there is an uneven amount of globin chain production, which results in an abundance of chains.. Read More»
    DOI: 10.37532/puljbdt.2022.5(6).5-6

 
Google Scholar citation report
Citations : 88

Journal of Blood Disorders and Treatment received 88 citations as per Google Scholar report

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