Article
Small deletions within the RHD coding sequence: a report of two novel mutational events and a survey of the underlying pathophysiologic mechanisms. Chen JM, Fichou Y, Jamet D, Dupont I, Cooper DN, Le Maréchal C, Férec C. Transfusion, 2013. [Citation]
Annotations by Allele
- RHD*29_42delGGCGCTGCCTGCCC: RH1 (mixed field agglutination, no RHCE variant could explain Rh1 epitopes)
- RHD*29_42delGGCGCTGCCTGCCC: Prevalence
- RHD*361_371delTTGTCGGTGCT or RHD*356_366delGTGCTTTGTCG (RHD*01N.41): RH1 (adsorption-elution was not performed)
- RHD*361_371delTTGTCGGTGCT or RHD*356_366delGTGCTTTGTCG (RHD*01N.41): otherHaplotype
- RHD*361_371delTTGTCGGTGCT or RHD*356_366delGTGCTTTGTCG (RHD*01N.41): Prevalence