Cooperating G6PD mutations associated with severe neonatal hyperbilirubinemia and cholestasis

Pediatric Blood and Cancer

Volumn 56, Issue 5, 2011, Pages 840-842

  Mizukawa, Benjamin ^a   George, Alex ^a   Pushkaran, Suvarnamala ^a   Weckbach, Lana ^a   Kalinyak, Karenann ^a   Heubi, James E ^a   Kalfa, Theodosia A ^a  

^a UNIVERSITY OF CINCINNATI COLLEGE OF MEDICINE   (United States)

Author keywords

Cholestasis; G6PD deficiency; Neonatal jaundice

Indexed keywords

GLUCOSE 6 PHOSPHATE DEHYDROGENASE;

ARTICLE; BLOOD SMEAR; CASE REPORT; CHOLESTASIS; CONTROLLED STUDY; EXTRAMEDULLARY HEMATOPOIESIS; GEL ELECTROPHORESIS; GENE MUTATION; GENE SEQUENCE; HEMOLYSIS; HEMOLYTIC ANEMIA; HEPATOSPLENOMEGALY; HUMAN; IMMUNOBLOTTING; INFANT; LIVER BIOPSY; LIVER INJURY; MALE; NEWBORN HEPATITIS; NEWBORN JAUNDICE; NUCLEOTIDE SEQUENCE; PHYSICAL EXAMINATION; PRIORITY JOURNAL; THROMBOCYTE TRANSFUSION;

AMINO ACID SEQUENCE; AMINO ACID SUBSTITUTION; CHOLESTASIS; DNA; GLUCOSEPHOSPHATE DEHYDROGENASE; GLUCOSEPHOSPHATE DEHYDROGENASE DEFICIENCY; HUMANS; HYPERBILIRUBINEMIA, NEONATAL; INFANT, NEWBORN; MALE; MOLECULAR SEQUENCE DATA; MUTATION; POLYMERASE CHAIN REACTION; SEQUENCE HOMOLOGY, AMINO ACID;

EID: 79952154990     PISSN: 15455009     EISSN: 15455017     Source Type: Journal    
DOI: 10.1002/pbc.22744     Document Type: Article

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