Molecular genetics of unconjugated hyperbilirubinemia in Taiwanese

Journal of Biomedical Science

Volumn 12, Issue 3, 2005, Pages 445-450

  Huang, Ching Shan ^a,b  

^a FOOYIN UNIVERSITY   (Taiwan)

^b CATHAY GENERAL HOSPITAL   (Taiwan)

Author keywords

Glucose 6 phosphate dehydrogenase; Organic anion transporter polypeptide 2; UDP glucuronosyltransferase 1A1; Unconjugated hyperbilirubinemia

Indexed keywords

BILIRUBIN; GLUCOSE 6 PHOSPHATE DEHYDROGENASE; NUCLEOTIDE;

ALLELE; ARTICLE; BILIRUBIN BLOOD LEVEL; BILIRUBIN METABOLISM; CANCER SUSCEPTIBILITY; CRIGLER NAJJAR SYNDROME; DNA POLYMORPHISM; GENE; GENE MUTATION; GENETIC RISK; GENETIC VARIABILITY; GILBERT DISEASE; GLUCOSE 6 PHOSPHATE DEHYDROGENASE DEFICIENCY; HAPLOTYPE; HETEROZYGOTE; HUMAN; MOLECULAR DYNAMICS; MOLECULAR GENETICS; ORGANIC ANION TRANSPORTER POLYPEPTIDE 2 GENE; PRIORITY JOURNAL; PROMOTER REGION; RISK FACTOR; TAIWAN;

ADULT; BILIRUBIN; CRIGLER-NAJJAR SYNDROME; GILBERT DISEASE; GLUCOSEPHOSPHATE DEHYDROGENASE DEFICIENCY; GLUCURONOSYLTRANSFERASE; HAPLOTYPES; HUMANS; HYPERBILIRUBINEMIA; HYPERBILIRUBINEMIA, HEREDITARY; MUTATION; NEOPLASMS; ORGANIC ANION TRANSPORT POLYPEPTIDE C; RISK FACTORS; TAIWAN; VARIATION (GENETICS);

EID: 22744458421     PISSN: 10217770     EISSN: 14230127     Source Type: Journal    
DOI: 10.1007/s11373-005-3863-5     Document Type: Article

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