Role of genetic screening in identifying susceptibility to acute fatty liver of pregnancy

Nature Clinical Practice Gastroenterology and Hepatology

Volumn 2, Issue 11, 2005, Pages 494-495

  Ibdah, Jamal A ^a  

^a University of Missouri   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

3 HYDROXYACYL COENZYME A DEHYDROGENASE; ACETYL COENZYME A ACYLTRANSFERASE; ACYL COENZYME A DEHYDROGENASE; ENOYL COENZYME A HYDRATASE; MITOCHONDRIAL PROTEIN;

CHEMICAL REACTION; DIAGNOSTIC VALUE; DIET THERAPY; DISEASE ASSOCIATION; DISEASE PREDISPOSITION; ENERGY RESOURCE; ENZYME DEFICIENCY; FATTY ACID OXIDATION; FATTY LIVER; GENE MUTATION; GENETIC COUNSELING; GENETIC SCREENING; HEART MUSCLE; HELLP SYNDROME; HUMAN; MATERNAL MORBIDITY; MATERNAL MORTALITY; NEWBORN SCREENING; PATHOGENESIS; PREGNANCY COMPLICATION; PRIORITY JOURNAL; REVIEW; SKELETAL MUSCLE; THIRD TRIMESTER PREGNANCY;

3-HYDROXYACYL COA DEHYDROGENASES; ACUTE DISEASE; FATTY LIVER; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENETIC SCREENING; HUMANS; INFANT, NEWBORN; MULTIENZYME COMPLEXES; NEONATAL SCREENING; PREGNANCY; PREGNANCY COMPLICATIONS;

EID: 31344477600     PISSN: 17434378     EISSN: 17434386     Source Type: Journal    
DOI: 10.1038/ncpgasthep0287     Document Type: Review

References (10)

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