Molecular and cellular characterization of a new α-Thalassemia mutation (HBA2:c.94A>C) generating an alternative splice site and a premature stop codon

T. Qadah, Jill Finlayson, C. Newbound, N. Pell, M. Pascoe, L. Greenwood, P. Holmes, D. Grey, Averil Beilby, Reza Ghassemifar

Research output: Contribution to journalArticle

3 Citations (Scopus)
Original languageEnglish
Pages (from-to)244-52
JournalHemoglobin
Volume36
Issue number3
DOIs
Publication statusPublished - 2012

Cite this

Qadah, T. ; Finlayson, Jill ; Newbound, C. ; Pell, N. ; Pascoe, M. ; Greenwood, L. ; Holmes, P. ; Grey, D. ; Beilby, Averil ; Ghassemifar, Reza. / Molecular and cellular characterization of a new α-Thalassemia mutation (HBA2:c.94A>C) generating an alternative splice site and a premature stop codon. In: Hemoglobin. 2012 ; Vol. 36, No. 3. pp. 244-52.
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Molecular and cellular characterization of a new α-Thalassemia mutation (HBA2:c.94A>C) generating an alternative splice site and a premature stop codon. / Qadah, T.; Finlayson, Jill; Newbound, C.; Pell, N.; Pascoe, M.; Greenwood, L.; Holmes, P.; Grey, D.; Beilby, Averil; Ghassemifar, Reza.

In: Hemoglobin, Vol. 36, No. 3, 2012, p. 244-52.

Research output: Contribution to journalArticle

TY - JOUR

T1 - Molecular and cellular characterization of a new α-Thalassemia mutation (HBA2:c.94A>C) generating an alternative splice site and a premature stop codon

AU - Qadah, T.

AU - Finlayson, Jill

AU - Newbound, C.

AU - Pell, N.

AU - Pascoe, M.

AU - Greenwood, L.

AU - Holmes, P.

AU - Grey, D.

AU - Beilby, Averil

AU - Ghassemifar, Reza

PY - 2012

Y1 - 2012

U2 - 10.3109/03630269.2012.670683

DO - 10.3109/03630269.2012.670683

M3 - Article

VL - 36

SP - 244

EP - 252

JO - Hemoglobin

JF - Hemoglobin

SN - 0363-0269

IS - 3

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