Simultaneous genotyping of human platelet alloantigen-1 to 28bw systems by multiplex polymerase chain reaction sequence-based typing
Author:
Affiliation:
1. Blood Center of Zhejiang Province; Hangzhou Zhejiang China
2. Key Laboratory of Blood Safety Research; Ministry of Health; Hangzhou Zhejiang China
3. Zhejiang Provincial Key Laboratory of Blood Safety Research; Hangzhou Zhejiang China
Funder
National Natural Science Foundation of China
Zhejiang Provincial Program for the Cultivation of High-Level Innovative Health Talents
Science Research Foundation of Zhejiang Healthy Bureau
Publisher
Wiley
Subject
Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/vox.12507/fullpdf
Reference30 articles.
1. A new low-frequency alloantigen (Kha(b)) located on platelet glycoprotein IIIa as a cause of maternal sensitization leading to neonatal alloimmune thrombocytopenia;Sullivan;Transfusion,2015
2. Further observations on the clinical significance and inheritance of the low-frequency platelet antigen HPA-28bw;Lucas;Transfusion,2016
3. Nomenclature of human platelet antigens;Metcalfe;Vox Sang,2003
4. Retrospective comparison of maternal vs. HPA-matched donor platelets for treatment of fetal alloimmune thrombocytopenia;Giers;Vox Sang,2010
5. Posttransfusion purpura occurrence and potential risk factors among the inpatient US elderly, as recorded in large Medicare databases during 2011 through 2012;Menis;Transfusion,2015
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