Associated Papers
Simultaneous genotyping for human platelet antigen systems and HLA-A and HLA-B loci by targeted next-generation sequencing.
Wang J et al.
Frontiers in Immunology, 2022
Case report: Two unique nonsense mutations in HTRA1-related cerebral small vessel disease in a Chinese population and literature review.
Chen W et al.
Frontiers in Neurology, 2022
36619910 (PubMed )
Supplement: Data_Sheet_6.ZIP › case2-C › 3.________ › CA2275B________.____Exonic_Variants.xlsx › sheet1
Identification of ITGA2B and ITGB3 Single-Nucleotide Polymorphisms and Their Influences on the Platelet Function.
Xiang Q et al.
Biomed Research International, 2016
Molecular pathology of rare bleeding disorders (RBDs) in India: a systematic review.
Kulkarni BP et al.
Plos One, 2014
Founder effect and estimation of the age of the French Gypsy mutation associated with Glanzmann thrombasthenia in Manouche families.
Fiore M et al.
European Journal of Human Genetics : Ejhg, 2011
Novel mutations in GP IIb gene in Glanzmann's thrombasthenia from India.
Vijapurkar M et al.
Platelets, 2009
New mutations on platelet GPIIb in Sub-Saharan African populations revealed by genotyping discrepancies.
Hallé L et al.
Transfusion, 2008
Linkage of four polymorphisms on the alphaIIb gene.
Ruan J et al.
British Journal of Haematology, 1998
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