In vitro characterization of the α-thalassemia point mutation HBA2:c.95+1G>A [IVS-I-1(G>A)(α2)]

T.H.W. Qadah, Jill Finlayson, Reza Ghassemifar

    Research output: Contribution to journalArticle

    8 Citations (Scopus)
    Original languageEnglish
    Pages (from-to)38-46
    JournalHemoglobin
    Volume36
    Issue number1
    DOIs
    Publication statusPublished - 2012

    Cite this

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    title = "In vitro characterization of the α-thalassemia point mutation HBA2:c.95+1G>A [IVS-I-1(G>A)(α2)]",
    author = "T.H.W. Qadah and Jill Finlayson and Reza Ghassemifar",
    year = "2012",
    doi = "10.3109/03630269.2011.599086",
    language = "English",
    volume = "36",
    pages = "38--46",
    journal = "Hemoglobin",
    issn = "0363-0269",
    publisher = "Informa Healthcare USA",
    number = "1",

    }

    In vitro characterization of the α-thalassemia point mutation HBA2:c.95+1G>A [IVS-I-1(G>A)(α2)]. / Qadah, T.H.W.; Finlayson, Jill; Ghassemifar, Reza.

    In: Hemoglobin, Vol. 36, No. 1, 2012, p. 38-46.

    Research output: Contribution to journalArticle

    TY - JOUR

    T1 - In vitro characterization of the α-thalassemia point mutation HBA2:c.95+1G>A [IVS-I-1(G>A)(α2)]

    AU - Qadah, T.H.W.

    AU - Finlayson, Jill

    AU - Ghassemifar, Reza

    PY - 2012

    Y1 - 2012

    U2 - 10.3109/03630269.2011.599086

    DO - 10.3109/03630269.2011.599086

    M3 - Article

    VL - 36

    SP - 38

    EP - 46

    JO - Hemoglobin

    JF - Hemoglobin

    SN - 0363-0269

    IS - 1

    ER -