D−− phenotype caused by a novel <scp><i>RHCE</i></scp> null allele-Reference-Cited by-同舟云学术

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D−− phenotype caused by a novel RHCE null allele

Published:2024-01-05 Issue:2 Volume:64 Page:
ISSN:0041-1132
Container-title:Transfusion
language:en
Short-container-title:Transfusion

Author:

Principi Cintia¹^ORCID,Trucco Boggione Carolina¹,Ensinck Alejandra¹,Posner Victoria¹,Luján Brajovich Melina¹,Stettler Silvina¹,Mattaloni Stella¹,Biondi Claudia¹,Cotorruelo Carlos¹

Affiliation:

1. Laboratorio de Inmunohematología e Inmunogenética, IDICER – CONICET Facultad de Ciencias Bioquímicas y Farmacéuticas, Universidad Nacional de Rosario Rosario Argentina

Funder

Agencia Nacional de Promoción Científica y Tecnológica

Universidad Nacional de Rosario

Publisher

Wiley

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/trf.17698

Reference4 articles.

1. Human Blood Groups

2. A convenient qualitative and quantitative method to investigateRHD-RHCEhybrid genes

3. Molecular characterization of rare D−−/D−− variants in individuals of Indian origin;Kulkarni S;Blood Transfus,2022

4. Study of the D-- phenotype reveals erythrocyte membrane alterations in the absence of RHCE

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Integrated analyses reveal unexpected complex inversion and recombination in RH genes;Blood Advances;2024-06-13

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