Rh(null) disease: The amorph type results from a novel double mutation in RhCe gene on D-negative background

Blood

Volumn 92, Issue 2, 1998, Pages 664-671

  Huang, Cheng Han ^a   Chen, Ying ^b   Reid, Marion E ^b   Seidl, Christine ^b  

^a NEW YORK BLOOD CENTER   (United States)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; BLOOD GROUP RHESUS SYSTEM; ERYTHROCYTE; GENE MUTATION; HEMOLYTIC ANEMIA; HUMAN; HUMAN TISSUE; PHENOTYPE; PRIORITY JOURNAL; RHESUS INCOMPATIBILITY; AMINO ACID SEQUENCE; FEMALE; GENETICS; MALE; MOLECULAR GENETICS; MUTATION; NUCLEOTIDE SEQUENCE; PEDIGREE;

CARRIER PROTEIN; CD47 ANTIGEN; CD47 PROTEIN, HUMAN; GLYCOPROTEIN; LEUKOCYTE ANTIGEN; MEMBRANE PROTEIN; PLASMA PROTEIN; RHAG PROTEIN, HUMAN; RHCE PROTEIN, HUMAN;

AMINO ACID SEQUENCE; ANTIGENS, CD; ANTIGENS, CD47; BASE SEQUENCE; BLOOD PROTEINS; CARRIER PROTEINS; FEMALE; GLYCOPROTEINS; HUMANS; MALE; MEMBRANE GLYCOPROTEINS; MOLECULAR SEQUENCE DATA; MUTATION; PEDIGREE; RH-HR BLOOD-GROUP SYSTEM;

EID: 0032527131     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.v92.2.664.414k27_664_671     Document Type: Article

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