Homozygous Point Mutations in Platelet Glycoprotein ITGA2B Gene as Cause of Glanzmann Thrombasthenia in 2 Families-Reference-Cited by-同舟云学术

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Homozygous Point Mutations in Platelet Glycoprotein ITGA2B Gene as Cause of Glanzmann Thrombasthenia in 2 Families

Published:2012-04 Issue:03 Volume:224 Page:174-178
ISSN:0300-8630
Container-title:Klinische Pädiatrie
language:de
Short-container-title:Klin Padiatr

Author:

Sandrock K.¹,Halimeh S.²,Wiegering V.³,Kappert G.²,Sauer K.⁴,Deeg N.¹,Busse E.¹,Zieger B.¹

Affiliation:

1. Departments of Pediatrics and Adolescent Medicine, University Hospital Freiburg, Germany

2. Coagulation Centre Rhine Ruhr, Duisburg, Germany

3. Department of Pediatric Hematology, Oncology and Neurooncology, University Children's Hospital Wuerzburg, Germany

4. Institute of Clinical Biochemistry and Pathobiochemistry - Central Laboratory, University Children's Hospital Wuerzburg, Germany

Publisher

Georg Thieme Verlag KG

Subject

Pediatrics, Perinatology, and Child Health

Link

http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0032-1306346.pdf

Cited by 4 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. In silico analysis of structural modifications in and around the integrin αIIb genu caused byITGA2Bvariants in human platelets with emphasis on Glanzmann thrombasthenia;Molecular Genetics & Genomic Medicine;2018-01-31

2. Molecular characterization of Glanzmann's thrombasthenia in Iran: identification of three novel mutations;BLOOD COAGUL FIBRIN;2017

3. Immunisation against αIIbβ3 and αvβ3 in a type 1 variant of Glanzmann’s thrombasthenia caused by a missense mutation Gly540Asp on β3;Thrombosis and Haemostasis;2016-03

4. Characterisation of patients with Glanzmann thrombasthenia and identification of 17 novel mutations;Thrombosis and Haemostasis;2015-07

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