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The intronic variant RHD :c.149−29G>C designated as RHD * 01EL.32 does not cause a DEL phenotype
Author(s) -
Kim Tae Yeul,
Yu HongBi,
Cho Duck
Publication year - 2021
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.16233
Subject(s) - medical genetics , medicine , medical school , medical laboratory , library science , medical education , genetics , biology , computer science , pathology , gene