A novel mutation in RHAG causing Rh null phenotype in Colombia-Reference-Cited by-同舟云学术

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A novel mutation in RHAG causing Rh null phenotype in Colombia

Published:2021-07-26 Issue:9 Volume:61 Page:
ISSN:0041-1132
Container-title:Transfusion
language:en
Short-container-title:Transfusion

Author:

Junca Tatiana Guerrero¹,Pinilla Jenny Johanna¹,Sanjuanelo Margaret¹,Lopez Katerynne¹,Dezan Marcia Regina²^ORCID,Peron Ana Cláudia³,Oliveira Valéria B.²,Conrado Marina C. A. V.²,Rocha Vanderson²⁴,Mendrone‐Júnior Alfredo²,Dinardo Carla Luana²⁵^ORCID

Affiliation:

1. Banco de Sangre, Servicio de Banco de Sangre Hospital Universitario de la Samaritana, Grupo de Investigación TRIBECA Bogota Colombia

2. Immunohematology Fundação Pró‐Sangue Hemocentro de São Paulo São Paulo Brazil

3. Immunohematology BIORAD Lagoa Santa Brazil

4. Department of Hematology Churchill Hospital, NHS BT, Oxford University Oxford UK

5. Tropical Hematology, Institute of Tropical Medicine Faculdade de Medicina da Universidade de São Paulo São Paulo Brazil

Publisher

Wiley

Subject

Hematology,Immunology,Immunology and Allergy

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/trf.16596

Reference7 articles.

1. Molecular genetic analysis of the Japanese amorph Rhnull phenotype

2. Characterization of the Ss sialoglycoprotein and its antigens in Rhnull erythrocytes

3. The presence of an RHD pseudogene containing a 37 base pair duplication and a nonsense mutation in Africans with the Rh D-negative blood group phenotype

4. A novel nonsense mutation in RHAG gene responsible for Rh null phenotype in a Chinese individual

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