No genetic abnormalities identified in α2IIb and β3: phenotype overcomes genotype in Glanzmann thrombasthenia-Reference-Cited by-同舟云学术

No genetic abnormalities identified in α2IIb and β3: phenotype overcomes genotype in Glanzmann thrombasthenia

Published:2016-11-03 Issue:2 Volume:39 Page:e41-e44
ISSN:1751-5521
Container-title:International Journal of Laboratory Hematology
language:en
Short-container-title:Int. Jnl. Lab. Hem.

Author:

Kannan M.¹,Saxena R.²

Affiliation:

1. Blood & Vascular Biology Research Laboratory; Department of Life Sciences; School of Basic and Applied Sciences; Central University of Tamil Nadu; Thiruvarur India

2. Department of Hematology; All India Institute of Medical Sciences; New Delhi India

Publisher

Wiley

Subject

Biochemistry, medical,Clinical Biochemistry,Hematology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/ijlh.12603/fullpdf

Reference13 articles.

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2. Molecular defects in ITGA2B and ITGB3 genes in patients with Glanzmann thrombasthenia;Kannan;J Thromb Haemost,2009

3. Presentation and pattern of symptoms in 382 patients with Glanzmann thrombasthenia in Iran;Toogeh;Am J Hematol,2004

4. Glanzmann thrombasthenia in Pakistan: molecular analysis and identification of novel mutations;Haghighi;Clin Genet,2016

5. The human integrin beta3 gene is 63 kb and contains a 5′-UTR sequence regulating expression;Wilhide;Blood,1997

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