Article
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.
Blood - 1 Jan 2000
Singleton B K, Green C A, Avent N D, Martin P G, Smart E, Daka A, Narter-Olaga E G, Hawthorne L M, Daniels G
Abstract excerpt
Antigens of the Rh blood group system are encoded by 2 homologous genes, RHD and RHCE, that produce 2 red cell membrane proteins. The D-negative phenotype is considered to result, almost invariably, from homozygosity for a complete deletion of RHD. The basis of all PCR tests for predicting fetal D phenotype from DNA obtained from amniocytes or maternal plasma is detection of the presence of RHD. These tests are...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.
