Literature DB >> 4846265

Absence of haemoglobin A in an individual simultaneously heterozygous in the genes for hereditary persistence of foetal haemoglobin and beta-thalassemia.

W M Fogarty, T S Vedvick, H A Itano.   

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Year:  1974        PMID： 4846265     DOI： 10.1111/j.1365-2141.1974.tb00496.x

Source DB:  PubMed          Journal:  Br J Haematol        ISSN： 0007-1048            Impact factor:   6.998


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  3 in total

1.  Therapeutic levels of fetal hemoglobin in erythroid progeny of β-thalassemic CD34+ cells after lentiviral vector-mediated gene transfer.

Authors:  Andrew Wilber; Phillip W Hargrove; Yoon-Sang Kim; Janice M Riberdy; Vijay G Sankaran; Eleni Papanikolaou; Maria Georgomanoli; Nicholas P Anagnou; Stuart H Orkin; Arthur W Nienhuis; Derek A Persons
Journal:  Blood       Date:  2010-12-14       Impact factor: 22.113

2.  Hereditary persistence of fetal hemoglobin, beta thalassemia, and the hemoglobin delta-beta locus: further family data and genetic interpretations.

Authors:  N C Bethlenfalvay; A G Motulsky; B Ringelhann; H Lehmann; J R Humbert; F I Konotey-Ahulu
Journal:  Am J Hum Genet       Date:  1975-03       Impact factor: 11.025

3.  SOX6 Downregulation Induces γ-Globin in Human β-Thalassemia Major Erythroid Cells.

Authors:  Jing Li; Yongrong Lai; Jun Luo; Lin Luo; Rongrong Liu; Zhenfang Liu; Weihua Zhao
Journal:  Biomed Res Int       Date:  2017-11-28       Impact factor: 3.411
  3 in total

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