UGT1 promoter polymorphism accounts for increased neonatal appearance of hereditary spherocytosis [3]

Blood

Volumn 91, Issue 3, 1998, Pages 1093-

  Iolascon, A ^a   Faienza, M F ^a   Moretti, A ^a   Perrotta, S ^a   Miraglia del Giudice, E ^a  

^a UNIVERSITY OF BARI   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ANEMIA; CLINICAL FEATURE; GENE INSERTION; GENE SEQUENCE; GENETIC POLYMORPHISM; HEREDITARY SPHEROCYTOSIS; HUMAN; JAUNDICE; LETTER; PATHOGENESIS; PRIORITY JOURNAL; PROMOTER REGION; SPLENOMEGALY; TATA BOX;

EID: 0032005254     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.v91.3.1093     Document Type: Letter

References (5)