DCS‐1, DCS‐2, and DFV share amino acid substitutions at the extracellular RhD protein vestibule
Willy A. Flegel(National Institutes of Health), Martin Pı́sačka(University of the West of England), Franz F. Wagner(DRK-Blutspendedienst Baden-Württemberg - Hessen), Jindra Vytisková(German Red Cross), Andrea Doescher(University of the West of England), Inge von Zabern(German Red Cross)
Cited by 28
Related Papers
Molecular Basis of Weak D Phenotypes
|Blood|1999|336
Molecular Basis of Weak D Phenotypes
|Blood|1999|331
RHD gene deletion occurred in the Rhesus box
|Blood|2000|319
RHD positive haplotypes in D negative Europeans
|BMC Genetics|2001|310
Weak D alleles express distinct phenotypes
|Blood|2000|255