Rare β-thalassemia mutations are cause of concern

被引：1

作者：

Gupta, A ^{[1
]}

Agarwal, S ^{[1
]}

机构：

[1] Sanjay Gandhi Postgrad Inst Med Sci, Dept Genet, Lucknow, Uttar Pradesh, India

来源：

AMERICAN JOURNAL OF HEMATOLOGY | 2004年 / 76卷 / 03期

关键词：

D O I：

10.1002/ajh.20084

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：312 / 312

页数：1

共 4 条

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[3] THE SAME TATA BOX BETA-THALASSEMIA MUTATION IN CHINESE AND UNITED-STATES BLACKS - ANOTHER EXAMPLE OF INDEPENDENT ORIGINS OF MUTATION [J].

HUANG, SZ ;

WONG, C ;

ANTONARAKIS, SE ;

TSAI, RL ;

LO, WHY ;

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[4] A novel β0-thalassemia mutation at codon 55 (-A) and a rare 17 bp deletion at codons 126-131 in the Indian population [J].

Nadkarni, A ;

Sakaguchi, T ;

Takaku, H ;

Gorakshakar, A ;

Phanasgaonkar, S ;

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Kiyama, R .

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