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A new RhD variant allele is caused by a RhD 26 T > G mutation in a Chinese Han woman with a weak D phenotype
Author(s) -
Qian Chunyan,
Li Qin,
Yuan Chao,
Bao Yinfeng,
Yu Shuli,
Li Shaoning,
Wang Yuejin,
Tao Zhihua,
Zhong Jiang
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.15135
Subject(s) - phenotype , allele , mutation , genetics , biology , gene
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