Association of ABO gene mutations resulting in a rare B subgroup


Autoria(s): Sousa, N.; Anicchino-Bizzacchi, J. M.; Leite, E. M.; Locatelli, M. F.; Albuquerque, D.; Costa, F. F.; Barjas-Castro, M. L.
Contribuinte(s)

Universidade Estadual Paulista (UNESP)

Data(s)

20/05/2014

20/05/2014

01/01/2005

Resumo

Background and Objectives B subgroups are rare and the genetic analysis reported to date has been limited.Materials and Methods Serological and molecular investigations were performed in blood from a B-subgroup donor.Results Red cells did not react with anti-B and anti-AB reagents. However, cells absorbed anti-B. Red cells presented positive reactions with anti-H, and saliva secreted H substance. The molecular study demonstrated a B allele with the substitutions 467C>T, 646T>A, 681G>A, 771C>T, 796C>A, 803G>C, 829G>A and an 0 allele with the sequence of 002.Conclusions It is probable that the presence in exon 7 of some of the 002 substitutions could have weakened the enzymatic activity of the encoded B transferase.

Formato

31-34

Identificador

http://dx.doi.org/10.1111/j.1423-0410.2005.00583.x

Vox Sanguinis. Oxford: Blackwell Publishing Ltd, v. 88, n. 1, p. 31-34, 2005.

0042-9007

http://hdl.handle.net/11449/7561

10.1111/j.1423-0410.2005.00583.x

WOS:000226931200005

Idioma(s)

eng

Publicador

Blackwell Publishing

Relação

Vox Sanguinis

Direitos

closedAccess

Palavras-Chave #ABO #B subgroup #blood group #genotyping #molecular biology
Tipo

info:eu-repo/semantics/article