| Literature DB >> 26175207 |
Carine Prisco Arnoni1, Janaína Guilhem Muniz1, Diana Gazito1, Rosangela de Medeiros Person1, Tatiane Aparecida de Paula Vendrame1, Lilian Castilho2, Flavia Roche Moreira Latini1.
Abstract
Rhnull is a rare phenotype characterized by the loss of Rh antigen expression. This phenotype can be related to several molecular backgrounds. In this study, we show a novel allele in a Brazilian pregnant woman encoding the Rhnull phenotype due to a change in RHAG exon2 c.310C>T, which leads to a premature stop codon (Gln104Stop).Entities:
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Year: 2015 PMID： 26175207 DOI： 10.1111/trf.13219
Source DB: PubMed Journal: Transfusion ISSN： 0041-1132 Impact factor: 3.157