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c.426G>C mutation in ABO*A1.02 allele was associated with Aw phenotype
Author(s) -
Chen Shu,
Hong Xiaozhen,
Xu Xianguo,
Ma Kairong,
He Ji,
Zhu Faming
Publication year - 2019
Publication title -
transfusion
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.045
H-Index - 132
eISSN - 1537-2995
pISSN - 0041-1132
DOI - 10.1111/trf.15496
Subject(s) - abo blood group system , allele , phenotype , genetics , mutation , biology , gene