RHD gene mutations and the weak D phenotype: An Australian blood donor study [7]

Vox Sanguinis

Volumn 79, Issue 4, 2000, Pages 251-252

  Cowley, Natalie M ^a   Saul, Allan ^b   Hyland, Catherine A ^a  

^a AUSTRALIAN RED CROSS BLOOD SERVICE   (Australia)

^b QIMR BERGHOFER MEDICAL RESEARCH INSTITUTE   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

RHESUS D ANTIGEN;

ANTIGEN EXPRESSION; BLOOD DONOR; CLINICAL ARTICLE; CONTROLLED STUDY; DNA SEQUENCE; ERYTHROCYTE; GENE EXPRESSION; GENE MUTATION; GENETIC ANALYSIS; HUMAN; LETTER; PHENOTYPE; PRIORITY JOURNAL;

AUSTRALIA; BLOOD DONORS; DNA MUTATIONAL ANALYSIS; HUMANS; PHENOTYPE; POINT MUTATION; RH-HR BLOOD-GROUP SYSTEM;

EID: 0034509717     PISSN: 00429007     EISSN: None     Source Type: Journal    
DOI: 10.1159/000056744     Document Type: Letter

References (5)

1. Defining the Rh blood group antigens. Biochemistry and molecular genetics
2. Molecular insights into the Rh protein family and associated antigens
3. N phenotypes
4. Lower antigen site density and weak D immunogenicity cannot be explained by structural genomic abnormalities or regulatory defects of the RHD gene
5. Molecular basis of weak D phenotypes