Rhnull phenotype caused by a novel RHAG mutation, c.945+1G>A, in the Japanese population.
Takashi UshikiHatsue TsuneyamaMasayoshi MasukoTakashi KozakaiTakuya KasamiTomoyuki TanakaMakoto UchikawaToshiki KitajimaEmiko KasaiTae KomataTakayuki KatagiriMasami KamimuraKenji SatoIchiro FuseKenichi OgasawaraKoh NakataPublished in: Transfusion (2019)
The mechanisms of hemolysis due to the Rhnull phenotype can vary, but our findings indicate that acute hemolytic crisis caused by the Rhnull syndrome could be associated with infection.