血红蛋白A2,经亚铁稳定 人

[ 外观性状 ]:
lyophilized powder

[ 储存条件 ]:
-20°C

[ 危害码 (欧洲) ]:
B

[ 危险品运输编码 ]:
NONH for all modes of transport

[ WGK德国 ]:
3

Prevalence of thalassaemia, iron-deficiency anaemia and glucose-6-phosphate dehydrogenase deficiency among Arab migrating nomad children, southern Islamic Republic of Iran.

East. Mediterr. Health J. 20(11) , 726-31, (2014)

This study investigated the prevalence of iron-deficiency anaemia, glucose-6-phosphate dehydrogenase (G6PD) deficiency and β-thalassaemia trait among Arab migrating nomad children in southern Islamic ...

Compromising for carrier detection of beta thalassemia based on measurement of HbA2 levels in unusual cases.

Clin. Chim. Acta 413(19-20) , 1705-7, (2012)

An increased HbA2 level is the hallmark for identification of β thalassemia carriers. However, in some carriers the level of HbA2 is not typically elevated creating difficulties in making a diagnosis....

α-thalassemia trait caused by frameshift mutations in exon 2 of the α2-globin gene: HBA2:c.131delT and HBA2:c.143delA.

Hemoglobin 36(5) , 511-5, (2012)

We describe two frameshift mutations associated with an α-thalassemia (α-thal) phenotype, identified in three unrelated individuals investigated for persistent microcytosis. The first mutation, HBA2:c...

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