Rapid Determination of α-Fetoprotein Gene Promoter Mutations in Hereditary Persistence of α-Fetoprotein
Author:
Affiliation:
1. Laboratoire d’Hormonologie et Biologie Moléculaire Hôpital Bicêtre AP-HP IFR93-Bicêtre, 78 rue du Général Leclerc, 94275 Le Kremlin-Bicêtre CEDEX, France
Publisher
Oxford University Press (OUP)
Subject
Biochemistry (medical),Clinical Biochemistry
Link
http://academic.oup.com/clinchem/article-pdf/50/9/1706/32732612/clinchem1706.pdf
Reference5 articles.
1. Hereditary persistence of α-fetoprotein is due to both proximal and distal hepatocyte nuclear factor-1 site mutations 1 1The authors thank Dr. A. Chauchereau for the gift of A9TKCAT vector, Dr. O. Lahuna for helpful discussion, C. Aumas for excellent technical assistance, and S. Wenk for careful English proofreading of the text. We are grateful for the cooperation of the patients and their families.
2. A G → A substitution in an HNF I binding site in the human α-fetoprotein gene is associated with hereditary persistence of α-fetoprotein (HPAFP)
3. Detection of Hereditary Persistence of α-Fetoprotein by Conformation-sensitive Gel Electrophoresis Analysis
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