References

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  5. Yukari Nishiyama et al. A case of suspected partial D because of weak reactivity to anti-D on column agglutination technology and identified as partial D (DBT-1) by genetic testing Japanese Journal of Transfusion and Cell Therapy, 2011. — Article — [RHeference]
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  8. Xu HY et al. [Identification of Phenotype and Genotype in One Case with Weak D blood group]. Zhongguo Shi Yan Xue Ye Xue Za Zhi, 2018. [Citation] [RHeference]
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  10. Qian C et al. A new RhD variant allele is caused by a RhD 26 T > G mutation in a Chinese Han woman with a weak D phenotype. Transfusion, 2019. [Citation] [RHeference]
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  12. Deng D et al. Identification of a novel c.94dupA mutation in RHD allele. Transfusion, 2020. [Citation] [RHeference]
  13. Lyu H et al. A novel RHD allele caused by c.739 G> C mutation was identified in a Chinese individual. Transfusion, 2021. [Citation] [RHeference]