Persistent α-Fetoprotein Elevation in Healthy Adults and Mutational Analysis of α-Fetoprotein Promoter, Enhancer, and Silencer Regions
Author:
Affiliation:
1. Department of Internal Medicine, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam, Korea
Funder
Seoul National University Hospital(SNUH)
Publisher
The Editorial Office of Gut and Liver
Subject
Gastroenterology,Hepatology
Link
http://pdf.medrang.co.kr/GNL/2017/011/ekjg011-01-21.pdf
Reference17 articles.
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2. Houwert, AC, Giltay, JC, Lentjes, EG, and Lock, MT (2010). Hereditary persistence of alpha-fetoprotein (HPAF P): review of the literature. Neth J Med. 68, 354-358.
3. Ferguson-Smith, MA, May, HM, O’Hare, E, and Aitken, DA (1983). Hereditary persistence of alphafetoprotein: a new autosomal dominant trait identified in an antenatal screening programme for spina bifida. J Med Genet. 20, 458.
4. Report of hereditary persistence of α-fetoprotein in a Spanish family: molecular basis and clinical concerns
5. Molecular mechanisms of hereditary persistence of α-fetoprotein (AFP) in two Japanese familiesA hepatocyte nuclear factor-1 site mutation leads to induction of the AFP gene expression in adult livers
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