Molecular characterization of thalassemia intermedia, due to co-inheritance of homozygous alpha triplication and IVSI-5 β-thalassemia

被引：7

作者：

Fallah, Mohammad-Sadegh ^{[2
,4
]}

Aleyasin, Seyed-Ahmad ^{[2
]}

Ebrahimi, Ahmad ^{[2
]}

Vakili, Azita Zadeh ^{[3
]}

Mahdian, Reza ^{[1
]}

Karimipour, Moretza ^{[1
]}

Jamali, Somayeh ^{[1
]}

Zeinali, Sirous ^{[1
,4
]}

Raeisi, Marzieh ^{[4
]}

Fooladi, Panti ^{[4
]}

Naderi, Majid ^{[5
]}

Baysal, Erol ^{[6
]}

机构：

[1] Pasteur Inst Iran, Dept Mol Med, Biotech Res Ctr, Tehran, Iran

[2] NIGEB, Tehran, Iran

[3] Ali Asghar Children Hosp, Prenatal Diag Lab, Zahedan, Iran

[4] Kawsar Human Genet Res Ctr, Tehran, Iran

[5] Zahedan Univ Med Sci, Dept Pediat, Zahedan, Iran

[6] Genet & Thalassemia Ctr, Dubai, U Arab Emirates

来源：

BLOOD CELLS MOLECULES AND DISEASES | 2009年 / 43卷 / 02期

关键词：

PHENOTYPES; SPECTRUM; IRAN;

D O I：

10.1016/j.bcmd.2009.05.006

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：158 / 160

页数：3

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