Heterozygous G71R-mutation causing Gilbert's syndrome in one of 103 random persons of German descent [1]

Journal of Hepatology

Volumn 42, Issue 5, 2005, Pages 778-779

  Sava, Marlis ^a   Kraemer, Doris M ^a  

^a UNIVERSITY OF WÜRZBURG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

GENOMIC DNA;

ADULT; ANALYZER; BILIRUBIN BLOOD LEVEL; BLOOD SAMPLING; CASE REPORT; DNA EXTRACTION; FRAMESHIFT MUTATION; G71R GENE; GENE; GENE MUTATION; GENETIC ANALYSIS; GERMANY; GILBERT DISEASE; HETEROZYGOSITY; HETEROZYGOTE DETECTION; HUMAN; HYPERBILIRUBINEMIA; LETTER; MALE; MISSENSE MUTATION; MUTATIONAL ANALYSIS; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; POPULATION RESEARCH; PRIORITY JOURNAL; PROGENY; PROMOTER REGION;

EID: 17044432138     PISSN: 01688278     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jhep.2004.11.045     Document Type: Letter

References (6)

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4. K. Akaba, T. Kimura, A. Sasaki, S. Tanabe, T. Ikegami, and M. Hashimoto Neonatal hyperbilirubinemia and mutation of the bilirubin uridine diphosphate glucuronosyltransferase gene: a common missense mutation among Japanese, Koreans and Chinese Biochem Mol Biol Int 46 1998 21 26
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