| Original language | English |
|---|---|
| Pages (from-to) | 244-52 |
| Journal | Hemoglobin |
| Volume | 36 |
| Issue number | 3 |
| DOIs | |
| Publication status | Published - 2012 |
Cite this
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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 journal › Article
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
ER -