A new RHD variant allele caused by an RHD c.1228-1G>C mutation in a Chinese family

Transfusion. 2021 Sep;61(9):E55-E56. doi: 10.1111/trf.16510. Epub 2021 Jul 22.

Authors

Fan Wu¹, Shuang Liang¹, Nai-Bao Zhuang¹, Yu-Qing Su¹, Yan-Lian Liang¹, Long Peng¹, Yun-Ping Xu¹, Chao-Peng Shao²

Affiliations

¹ Institute of Transfusion Medicine, Shenzhen Blood Center, Shenzhen, China.
² Department of Blood Transfusion, The First Affiliated Hospital of Shenzhen University School of Medicine, The Second People's Hospital of Shenzhen, Shenzhen, China.

PMID: 34291823
DOI: 10.1111/trf.16510

No abstract available

Publication types

Case Reports
Research Support, Non-U.S. Gov't

MeSH terms

Alleles
Asian People / genetics
Female
Humans
Male
Mutation
Pedigree
Polymorphism, Single Nucleotide
Rh-Hr Blood-Group System / genetics*

Substances

Rh-Hr Blood-Group System
Rho(D) antigen