2010
DOI: 10.1111/j.1537-2995.2010.02611.x
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RHD positive among C/E+ and D− blood donors in Denmark

Abstract: Of 233 donors analyzed, seven were found positive for RHD Exon 10, and four of these were Del, corresponding to 1.7%. We report here a new mutation in the RHD gene. A correct assignment of all blood donors as D+ or D- is not possible using serotyping alone; genotyping offers the only exact categorization of all cases.

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Cited by 24 publications
(29 citation statements)
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“…The Rh antigens are also the most clinically significant in transfusion medicine [1,2]. They are located on two proteins, RhD and RhCE: the former carries the D antigen, while the latter carries C, c, E, and e antigens.…”
Section: Brief Communication (Original)mentioning
confidence: 99%
See 1 more Smart Citation
“…The Rh antigens are also the most clinically significant in transfusion medicine [1,2]. They are located on two proteins, RhD and RhCE: the former carries the D antigen, while the latter carries C, c, E, and e antigens.…”
Section: Brief Communication (Original)mentioning
confidence: 99%
“…Several RH D, RH C/c, and RH E/e genotyping assays have been developed. A number of studies have been carried out to assess the frequency of these three molecular backgrounds in people of African and Caucasian ancestry [2,8].…”
Section: Brief Communication (Original)mentioning
confidence: 99%
“…Although the main RHD alleles resulting in a D- phenotype, i.e. RHDΨ and (C)ce s , are most frequently cis -associated with RHCE*ce , other RHD gene variants in D- individuals, including several hybrid genes, have been shown to segregate with RHCE alleles expressing C and/or E (C/E+) antigens in Caucasian, Asian, African, and mixed populations [4,7,8,9,10,11,12,13,14,15,16,17,18,19,20]. …”
Section: Introductionmentioning
confidence: 99%
“…Generally, the frequency of DEL among Europeans is 1:350 to 1:2,000, while it gets as high as 1:5 among Asians. It should be noted that in many studies [8,23,47,56] weak D or partial D donors were detected among donors previously believed to be D-negative.…”
Section: Frequency Of Missed D-positive Samplesmentioning
confidence: 99%
“…Since most DEL and weak D differ from normal RHD by splice site or missense mutations, they are not affected by this problem, and testing for almost any RHD -specific polymorphism will reveal the vast majority of DEL samples. Therefore, if sensitive serologic testing is continued to detect partial D caused by hybrid alleles, testing a single RHD polymorphism by PCR may be a possible choice to find the DEL samples [28,35,47]. …”
Section: Which Rhd Pcr Should Be Used?mentioning
confidence: 99%