The intronic variant RHD:c.149-29G>C designated as RHD*01EL.32 does not cause a DEL phenotype

Transfusion. 2021 Mar;61(3):986-987. doi: 10.1111/trf.16233.

Authors

Tae Yeul Kim¹, HongBi Yu², Duck Cho^{1

2}

Affiliations

¹ Department of Laboratory Medicine and Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.
² Department of Health Sciences and Technology, Samsung Advanced Institute for Health Sciences and Technology, Sungkyunkwan University, Seoul, South Korea.

PMID: 33719044
DOI: 10.1111/trf.16233

No abstract available

Publication types

Letter
Comment

MeSH terms

Alleles
Mutation
Phenotype
Rh-Hr Blood-Group System* / genetics

Substances

Rh-Hr Blood-Group System