• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

The spectrum of beta-thalassaemia mutations on the Indian subcontinent: the basis for prenatal diagnosis.

作者信息

Varawalla N Y, Old J M, Sarkar R, Venkatesan R, Weatherall D J

机构信息

Institute of Molecular Medicine, John Radcliffe Hospital, Oxford.

出版信息

Br J Haematol. 1991 Jun;78(2):242-7. doi: 10.1111/j.1365-2141.1991.tb04423.x.

DOI:10.1111/j.1365-2141.1991.tb04423.x
PMID:2064964
Abstract

The beta-thalassaemia mutations in 702 unrelated carriers originating from seven different regions of the Indian subcontinent have been characterized using allele specific priming of the polymerase chain reaction (PCR). It was possible to identify the mutations in 688 (98%) of the individuals studied. Eleven different mutations were identified, of which five common ones accounted for 93.6%; namely the ones at IVS-1 position 5 (G-C), codons 8/9 (+G), IVS-1 position 1 (G-T), codons 41/42 (-CTTT) and the 619 bp deletion at the 3' end of the gene. The mutations at IVS-2 position 1 (G-A) and codon 30 (G-C), previously undescribed in Asian Indians, were found in two and six individuals respectively. Some regional variation in the distribution of beta-thalassaemia alleles was noted. These findings should prove useful for the development of a first trimester prenatal diagnosis programme based on direct detection of mutations.

摘要

相似文献

1
The spectrum of beta-thalassaemia mutations on the Indian subcontinent: the basis for prenatal diagnosis.
Br J Haematol. 1991 Jun;78(2):242-7. doi: 10.1111/j.1365-2141.1991.tb04423.x.
2
Rare beta-thalassaemia mutations in Asian indians.
Br J Haematol. 1991 Dec;79(4):640-4. doi: 10.1111/j.1365-2141.1991.tb08094.x.
3
Prenatal diagnosis and control strategies for beta-thalassaemia on the Indian subcontinent.印度次大陆β地中海贫血的产前诊断与控制策略
Natl Med J India. 1992 Jul-Aug;5(4):157-61.
4
The spectrum of beta-thalassemia mutations in southern Thailand.泰国南部β地中海贫血突变谱。
Southeast Asian J Trop Med Public Health. 1995;26 Suppl 1:229-34.
5
Analysis of beta-globin gene haplotypes in Asian Indians: origin and spread of beta-thalassaemia on the Indian subcontinent.亚洲印度人β-珠蛋白基因单倍型分析:β地中海贫血在印度次大陆的起源与传播
Hum Genet. 1992 Dec;90(4):443-9. doi: 10.1007/BF00220475.
6
Molecular basis of beta-thalassemia in Thailand: analysis of beta-thalassemia mutations using the polymerase chain reaction.泰国β地中海贫血的分子基础:利用聚合酶链反应分析β地中海贫血突变
Hum Genet. 1989 Dec;84(1):41-6. doi: 10.1007/BF00210668.
7
The spectrum of beta thalassaemia in Burma.
Br J Haematol. 1992 Aug;81(4):574-8. doi: 10.1111/j.1365-2141.1992.tb02994.x.
8
Regional distribution of beta-thalassemia mutations in India.印度β地中海贫血突变的区域分布。
Hum Genet. 1997 Jul;100(1):109-13. doi: 10.1007/s004390050475.
9
The spectrum of beta thalassaemia mutations in the UAE national population.阿联酋国民群体中β地中海贫血突变的谱系
J Med Genet. 1994 Jan;31(1):59-61. doi: 10.1136/jmg.31.1.59.
10
The molecular basis of beta-thalassemia in Thailand: application to prenatal diagnosis.泰国β地中海贫血的分子基础:在产前诊断中的应用
Am J Hum Genet. 1990 Sep;47(3):369-75.

引用本文的文献

1
Prevalence of β-thalassaemia trait among school-going children in Jawadhi Hills: A School-based cross-sectional study.贾瓦迪山学龄儿童中β地中海贫血特征的患病率:一项基于学校的横断面研究。
J Family Med Prim Care. 2025 Jun;14(6):2226-2230. doi: 10.4103/jfmpc.jfmpc_1296_24. Epub 2025 Jun 30.
2
Genetic disease risks of under-represented founder populations in New York City.纽约市代表性不足的奠基人群体的遗传疾病风险。
PLoS Genet. 2025 Jun 24;21(6):e1011755. doi: 10.1371/journal.pgen.1011755. eCollection 2025 Jun.
3
Genetic landscape and hematological profiling of thalassemia in patients from the Malwa region, Central India.
印度中部马尔瓦地区地中海贫血患者的基因图谱与血液学分析
Mol Genet Genomics. 2025 Apr 12;300(1):42. doi: 10.1007/s00438-025-02245-7.
4
Newborn Screening in Developing Countries: The Need of the Hour.发展中国家的新生儿筛查:当务之急
Cureus. 2024 May 3;16(5):e59572. doi: 10.7759/cureus.59572. eCollection 2024 May.
5
Spectrum of Rare and Novel Indel Mutations Responsible for β Thalassemia in Eastern India.印度东部导致β地中海贫血的罕见和新型插入缺失突变谱。
Indian J Clin Biochem. 2024 Apr;39(2):207-213. doi: 10.1007/s12291-022-01098-w. Epub 2023 Jan 3.
6
Compound Heterozygous for Asian Inversion Deletion Gγ (Aγδβ) and IVS1-5 (G→C) β Thalassemia Mutation in a Transfusion-Dependent Patient.一名依赖输血的患者中亚洲人γ珠蛋白基因倒位缺失(Aγδβ)和IVS1-5(G→C)β地中海贫血突变的复合杂合子。
Indian J Pediatr. 2024 Mar;91(3):309. doi: 10.1007/s12098-023-04825-0. Epub 2023 Sep 14.
7
A community based study on haemoglobinopathies and G6PD deficiency among particularly vulnerable tribal groups in hard-to-reach malaria endemic areas of Odisha, India: implications on malaria control.印度奥里萨邦疟疾流行的偏远地区针对特定弱势群体的血红蛋白病和 G6PD 缺乏症的社区研究:对疟疾控制的影响。
Malar J. 2022 Nov 16;21(1):340. doi: 10.1186/s12936-022-04358-5.
8
Rapid molecular identification of a rare gene deletion & its clinical implication.一种罕见基因缺失的快速分子鉴定及其临床意义。
Indian J Med Res. 2022 Mar;155(3&4):432-437. doi: 10.4103/ijmr.IJMR_4753_20.
9
Molecular basis and diagnosis of thalassemia.地中海贫血的分子基础与诊断
Blood Res. 2021 Apr 30;56(S1):S39-S43. doi: 10.5045/br.2021.2020332.
10
A demographic prevalence of β Thalassemia carrier and other hemoglobinopathies in adolescent of Tharu population.塔鲁族青少年中β地中海贫血携带者和其他血红蛋白病的人口统计学患病率。
J Family Med Prim Care. 2020 Aug 25;9(8):4305-4310. doi: 10.4103/jfmpc.jfmpc_879_20. eCollection 2020 Aug.