http://rdf.ncbi.nlm.nih.gov/pubchem/reference/9493085

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contentType Case Reports|Journal Article|Research Support, Non-U.S. Gov't
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publicationName Transfusion
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bibliographicCitation Hong X, Chen S, Ma K, He J, Zhu F. c.830T>C mutation on the ABO*A1.02 allele responsible for Aw phenotype. Transfusion. 2019 Oct;59(10):E11–2. doi: 10.1111/trf.15413. PMID: 31240718.
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date 2019-06-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier https://pubmed.ncbi.nlm.nih.gov/31240718
https://doi.org/10.1111/trf.15413
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language English
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title c.830T>C mutation on the ABO*A1.02 allele responsible for Aw phenotype
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Total number of triples: 33.