期刊文献+

罕见β地中海贫血基因-86(C〉G)突变家系的分子诊断 被引量:7

原文传递
导出
摘要 β-地中海贫血(简称0.地贫)是世界上最常见的单基因遗传病之一,全球约有1.8亿人携带此类基因,在我国南方广西和广东地区人群中携带率高达6.43%和2.54%。β-地贫是由于β珠蛋白基因突变导致β珠蛋白链合成减少或缺如所引起的溶血性贫血,
出处 《中华检验医学杂志》 CAS CSCD 北大核心 2013年第5期438-440,共3页 Chinese Journal of Laboratory Medicine
基金 百色市科学研究与技术开发项目(百科计20111220)
  • 相关文献

参考文献9

  • 1Modella B, Darlisona M. Global epidemiology of haemoglobin disorders and derived service indicators. Bulletin World Health Organ, 2008, 86:480-487.
  • 2Weatberall DJ, Williams TN, Allen SJ, et al. The population genetics and dynamics of the thalassemias. Hematol Oncol Clin Noah Am, 2010, 24:1021-1031.
  • 3Xu XM, Zhou YQ, Luo CX, et al. The privalence anti spectrum of a and β thalassemia in Ghangdong Province:implications for the future health burden and population screening. J Clin Pathol, 2004, 57:517-522.
  • 4Xiong F, Sun M, Zhang X, et al. Molecular epidemiological survey of haemoglobinopathies in the Guangxi Zhuang Autonomous Region of southern China. Clin Genet, 2010, 78:139-148.
  • 5Huang H, Xu L, Lin N, et al. A new beta-thalassemia deletion mutation [ codon 36 (-C)] observed in a Chinese woman. Hemoglobin, 2010, 34:599-603.
  • 6Harteveld CL, Kleanthous M, Traeger-Synodinos J. Prenata diagnosis of hemoglobin disorders: present and future strategies. Clin Biochem, 2009, 42:1767-1779.
  • 7Galanello R, Origa R. Beta-thalassemia. Orphanet J Rare Dis 2010, 5:11.
  • 8Yao H, Chert Z, Su Q, et al. Erythrocyte membrane protein abnormalities in beta thalassemia of the Li nationality in Hainarl. Chin Med J, 2001, 114:486-488.
  • 9Kazazian HH. The thalassemia syndromes: molecular basis and prenatal diagnosis in 1990. Semin Hematol, 1990, 27:209-228.

同被引文献70

  • 1许涓涓,杜娟,唐斌,蒙达华,李萌,谭舒尹,黄萍丽.泰国缺失型α-地中海贫血基因诊断和误诊分析[J].中华临床医师杂志(电子版),2012,6(16):4921-4922. 被引量:8
  • 2陈萍,李树全,李敏清,庞丽红,林伟雄.泰国缺失型α地中海贫血1的产前基因诊断[J].中华医学遗传学杂志,2007,24(3):247-250. 被引量:24
  • 3张力,区小冰,余一平.广东地区中间型β地中海贫血的基因分析[J].中国当代儿科杂志,2007,9(4):358-360. 被引量:5
  • 4许文荣,王建中.临床血液学与检验[M].北京:人民卫生出版社,2008:273-274.
  • 5Long J, Yah K, et al.the diagnosis and molecular analysis of a novel 21.9kb deleteon (Qinzhou type deletion) causing ct+thalassemia[J]. Blood Cells Mol Dis, 2014, 52 (4) .225-229.
  • 6Xiao-Feng Wei, Xuan Shang, De-Qin He, et al. Molecular charac terization of a novel 27.6-kbdeletion causing α'thalassemia in a Chinese family[J].Ann Haematol, 2011,90 ( 1 ) : 17-22.
  • 7Giardine B, van Baal S, Kaimakis P, et al. HbVar database of human hemoglobin variants and thalassemia mutations: 2007 update[J]. Hum Murat,2007,28 ( 2 ) :206-215.
  • 8Li DZ, Liao C, Xie XM, et al. A novel nmtation of-50 ( G > A ) in the direct repeat element of the beta-globin gene identified in a patient with severe beta-thalassemia [ J ]. Ann Hematol, 2009,88 ( 11 ) : 1149-1150. DOI : 10. 1007/s00277-009-0732-8.
  • 9Huang H, Xu L, Lin N, et al. A new deletion [3-thalassemia mutation[ codon 36 (-c)] found in a Chinese woman [ J]. Hemoglobin ,2010,34 (6) :599-603.
  • 10Taher A, Isma' eel H, Cappellini MD. Thalassemia intermedia: revisited [ J ]. Blood Cells Mol Dis,2006,37 ( 1 ) : 12-20.

引证文献7

二级引证文献22

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部