A nait‐associated and previously unreported mutation in the ITGB3 gene with a low frequency in the local population
Author:
Affiliation:
1. DRK‐Blutspendedienst NSTOB Institut Bremen‐Oldenburg Oldenburg Germany
2. DRK‐Blutspendedienst NSTOB Institut Springe Springe Germany
3. St. Marienhospital Vechta Vechta Germany
Publisher
Wiley
Subject
Hematology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/tme.12769
Reference26 articles.
1. Human platelet antigen-specific alloantibodies implicated in 1162 cases of neonatal alloimmune thrombocytopenia
2. A new Ser472Asn (Cab2a+) polymorphism localized within the αIIb “thigh” domain is involved in neonatal thrombocytopenia
3. The αIIb p.Leu841Met (Cab3a+) polymorphism results in a new human platelet alloantigen involved in neonatal alloimmune thrombocytopenia
4. Immunization against a low-frequency human platelet alloantigen in fetal alloimmune thrombocytopenia is not a single event: characterization by the combined use of reference DNA and novel allele-specific cell lines expressing recombinant antigens
5. New platelet glycoprotein polymorphisms causing maternal immunization and neonatal alloimmune thrombocytopenia
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1. A nait‐associated and previously unreported mutation in the ITGB3 gene with a low frequency in the local population;Transfusion Medicine;2021-03-16
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