The human Rh50 glycoprotein gene: Structural organization and associated splicing defect resulting in Rh(null) disease

Journal of Biological Chemistry

Volumn 273, Issue 4, 1998, Pages 2207-2213

  Huang, Cheng Han ^a  

^a NEW YORK BLOOD CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GLYCOPROTEIN; RHESUS ANTIBODY;

ARTICLE; BLOOD GROUP RHESUS SYSTEM; CARBOXY TERMINAL SEQUENCE; CHROMOSOME 1P; ERYTHROCYTE MEMBRANE; GENE LOCATION; GENE MUTATION; HEREDITARY HEMOLYTIC ANEMIA; HUMAN; HUMAN CELL; NUCLEIC ACID BASE SUBSTITUTION; NUCLEOTIDE SEQUENCE; PATHOGENESIS; PRIORITY JOURNAL; PROTEIN PROTEIN INTERACTION; RNA SPLICING; SPHEROCYTOSIS;

AMINO ACID SEQUENCE; BASE SEQUENCE; BLOOD PROTEINS; EXONS; GLYCOPROTEINS; HUMANS; INTRONS; MEMBRANE GLYCOPROTEINS; MOLECULAR SEQUENCE DATA; MUTAGENESIS; PHENOTYPE; RH-HR BLOOD-GROUP SYSTEM; RNA SPLICING;

EID: 0031953137     PISSN: 00219258     EISSN: None     Source Type: Journal    
DOI: 10.1074/jbc.273.4.2207     Document Type: Article

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