ABCB4 gene mutations and single-nucleotide polymorphisms in women with intrahepatic cholestasis of pregnancy

Journal of Medical Genetics

Volumn 46, Issue 10, 2009, Pages 711-715

  Bacq, Y ^a,c   Gendrot, C ^a   Perrotin, F ^a   Lefrou, L ^a   Chretien S ^a   Vie Buret, V ^a   Brechot, M C ^a   Andres, C R ^a,b  

^a UNIVERSITY HOSPITAL OF TOURS   (France)

^b UNIVERSITÉ DE TOURS   (France)

^c SERVICE DE DERMATOLOGIE   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ALANINE AMINOTRANSFERASE; BILE ACID; DNA;

ABC TRANSPORTER B4 GENE; ADULT; ALANINE AMINOTRANSFERASE BLOOD LEVEL; ALLELE; ARTICLE; CAUCASIAN; CONTROLLED STUDY; CONVALESCENCE; DELIVERY; DNA SEQUENCE; ENZYME ACTIVITY; FEMALE; GENE; GENE MUTATION; GENETIC ASSOCIATION; GENETIC VARIABILITY; GENOMICS; HAPLOTYPE; HETEROZYGOSITY; HUMAN; INTRAHEPATIC CHOLESTASIS; MAJOR CLINICAL STUDY; MISSENSE MUTATION; NONHUMAN; NONSENSE MUTATION; PATHOGENESIS; PREGNANCY; PRIORITY JOURNAL; PROSPECTIVE STUDY; PRURITUS; SINGLE NUCLEOTIDE POLYMORPHISM;

ADULT; AMINO ACID SEQUENCE; CHOLESTASIS, INTRAHEPATIC; FEMALE; GENE FREQUENCY; HUMANS; MOLECULAR SEQUENCE DATA; MUTATION; P-GLYCOPROTEINS; POLYMORPHISM, SINGLE NUCLEOTIDE; PREGNANCY; PREGNANCY COMPLICATIONS; PROSPECTIVE STUDIES; SEQUENCE ALIGNMENT;

EID: 70349656641     PISSN: 00222593     EISSN: 14686244     Source Type: Journal    
DOI: 10.1136/jmg.2009.067397     Document Type: Article

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