Abstract
Rhnull blood type is characterized by the complete absence of Rh antigens on red blood cells, a condition that can lead to notable morphological abnormalities. In this study, a patient with an Rhnull phenotype was identified through serologic testing. Sequencing of RHAG revealed a novel c.640+1G>C mutation, which was subsequently confirmed to be inherited from the father and transmitted to the children.
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Authors
Min Wang Department of Blood Transfusion, the First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui, China; Organ Transplant Center, the First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui, China
Shuangshuang Jia Institute of Blood Transfusion and Hematology, Guangzhou Blood Center, Guangzhou Medical University, Guangzhou, China
Shanshan Zhou Department of Blood Transfusion, the First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui, China
Shihui Li Organ Transplant Center, the First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui, China
Qian Liu
Organ Transplant Center, the First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui, China
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