Lack of common mutation in the alfa-subunit of the mitochondrial trifunctional protein and the polymorphism of CYP2E1 in three Japanese women with acute fatty liver of pregnancy/HELLP syndrome

Hepatology Research

Volumn 30, Issue 4, 2004, Pages 226-231

  Fukushima, Koji ^a   Ueno, Yoshiyuki ^a   Inoue, Jun ^a   Kanno, Noriatsu ^a   Nagasaki, Futoshi ^a   Mikami, Emiko ^a   Moritoki, Yuki ^a   Kondo, Yasuteru ^a   Shimosegawa, Tooru ^a  

^a TOHOKU UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

AFLP; Fatty acid; LCHAD; liver disease; Pregnancy

Indexed keywords

ACETYL COENZYME A ACYLTRANSFERASE; CYTOCHROME P450 2E1; ENOYL COENZYME A HYDRATASE; GENOMIC DNA;

ADULT; ALPHA CHAIN; ARTICLE; CASE REPORT; CORRELATION ANALYSIS; DNA EXTRACTION; DNA FLANKING REGION; FEMALE; GENE MUTATION; HELLP SYNDROME; HOMOZYGOSITY; HUMAN; INCIDENCE; JAPAN; LIVER FATTY DEGENERATION; POLYMERASE CHAIN REACTION; PREVALENCE; PRIORITY JOURNAL; PROTEIN POLYMORPHISM; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; RISK FACTOR; WILD TYPE;

EID: 10944266506     PISSN: 13866346     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.hepres.2004.09.005     Document Type: Article

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