In vitro characterization of the α-thalassemia point mutation HBA2:c.95+1G>A [IVS-I-1(G>A) (α2)].
about
Molecular characterization of Hb Hamilton Hill (HBA2: c.388delC), a novel HBA2 variant generating a premature termination codon and truncated HBA2 chain.Identification of Mutations Causing Aberrant Termination and Deficient Splice Donor Site on the HBA1 Gene.Molecular and cellular analysis of a novel HBA2 mutation (HBA2: c.94A > G) shows activation of a cryptic splice site and generation of a premature termination codon.
P2860
In vitro characterization of the α-thalassemia point mutation HBA2:c.95+1G>A [IVS-I-1(G>A) (α2)].
description
2011 nî lūn-bûn
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2011年の論文
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2011年論文
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name
In vitro characterization of the α-thalassemia point mutation HBA2:c.95+1G>A [IVS-I-1
@nl
In vitro characterization of t ...... c.95+1G>A [IVS-I-1(G>A) (α2)].
@en
type
label
In vitro characterization of the α-thalassemia point mutation HBA2:c.95+1G>A [IVS-I-1
@nl
In vitro characterization of t ...... c.95+1G>A [IVS-I-1(G>A) (α2)].
@en
prefLabel
In vitro characterization of the α-thalassemia point mutation HBA2:c.95+1G>A [IVS-I-1
@nl
In vitro characterization of t ...... c.95+1G>A [IVS-I-1(G>A) (α2)].
@en
P2093
P2860
P1433
P1476
In vitro characterization of t ...... c.95+1G>A [IVS-I-1(G>A) (α2)].
@en
P2093
Jill Finlayson
Reza Ghassemifar
Talal Qadah
P2860
P356
10.3109/03630269.2011.599086
P577
2011-10-03T00:00:00Z