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

doi:10.3109/03630269.2012.670683

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 journal › Article › peer-review

3 Citations (Scopus)

Original language	English
Pages (from-to)	244-52
Journal	Hemoglobin
Volume	36
Issue number	3
DOIs	https://doi.org/10.3109/03630269.2012.670683
Publication status	Published - 2012

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10.3109/03630269.2012.670683

Cite this

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

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

year = "2012",

doi = "10.3109/03630269.2012.670683",

language = "English",

volume = "36",

pages = "244--52",

journal = "Hemoglobin",

issn = "0363-0269",

publisher = "Informa Healthcare USA",

number = "3",

}

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

C2 - 22524210

SN - 0363-0269

VL - 36

SP - 244

EP - 252

JO - Hemoglobin

JF - Hemoglobin

IS - 3

ER -