Varaico: Literature-Extracted Genetic Variants

Gene:RHD
Variant:p.S122L
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RHD

NM_016124.6:p.S122L

Associated Papers

Transfusion management of Africans with RHD variants in China.

Yin Q et al.

Transfusion Clinique Et Biologique : Journal De La Societe Francaise De Transfusion Sanguine, 2023

RHD alleles contributing to serologically weak D phenotypes in China: A single-centre study over 10 years.

Ye L et al.

Vox Sanguinis, 2022

The Significance of RHD Genotyping and Characteristic Analysis in Chinese RhD Variant Individuals.

Ying Y et al.

Frontiers in Immunology, 2021

Molecular and computational analysis of 45 samples with a serologic weak D phenotype detected among 132,479 blood donors in northeast China.

Zhang X et al.

Journal of Translational Medicine, 2019

Prevalence of RHD alleles in Japanese individuals with weak D phenotype: Identification of 20 new RHD alleles.

Isa K et al.

Vox Sanguinis, 2016

[Molecular genetic analysis of a weak D phenotype].

Lin F et al.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics, 2014

The RHCE allele ceSL: the second example for D antigen expression without D-specific amino acids.

Chen Q et al.

Transfusion, 2006

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."