mRNA metabolism of β-globin genes carrying premature translational stop mutations. A molecular basis for the recessive and dominant modes of inheritance of β-thalassemia?

International Journal of Pediatric Hematology/Oncology

Volumn 4, Issue 5, 1997, Pages 499-511

  Kulozik, A E ^a   Kugler, W ^a   Enssle, J ^a   Hentze, M W ^a  

^a HUMBOLDT UNIVERSITY   (Germany)

Author keywords

globin genes; thalassemia; Nonsense mediated mRNA decay

Indexed keywords

BETA GLOBIN; MESSENGER RNA;

ARTICLE; AUTOSOMAL RECESSIVE INHERITANCE; BETA THALASSEMIA; CARBOXY TERMINAL SEQUENCE; CONTROLLED STUDY; ERYTHROID CELL; GENE EXPRESSION; GENE MUTATION; GENETIC TRANSFECTION; HELA CELL; HETEROZYGOSITY; HUMAN; HUMAN CELL; INHERITANCE; INTRON; MOLECULAR GENETICS; NONSENSE MUTATION; NORTHERN BLOTTING; PHENOTYPE; PRIORITY JOURNAL; PROMOTER REGION; RNA DEGRADATION; RNA METABOLISM; STEM CELL; STOP CODON;

EID: 0031455046     PISSN: 10702903     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (27)