Molekulare Diagnostik bei genetischen Lebererkrankungen
Author:
Publisher
Springer Science and Business Media LLC
Subject
Gastroenterology
Link
http://link.springer.com/content/pdf/10.1007/s11377-010-0487-8.pdf
Reference29 articles.
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3. Hadj-Rabia S, Baala L, Vabres P et al (2004) Claudin-1 gene mutations in neonatal sclerosing cholangitis associated with ichthyosis: a tight junction disease. Gastroenterology 127: 1386–1390
4. Stapelbroek JM, Erpecum KJ van, Klomp LW, Houwen RH (2010) Liver disease associated with canalicular transport defects: current and future therapies. J Hepatol 52: 258–271
5. Gotthardt D, Runz H, Keitel V et al (2008) A mutation in the canalicular phospholipid transporter gene, ABCB4, is associated with cholestasis, ductopenia, and cirrhosis in adults. Hepatology 48: 1157–1166
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