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Indel in the FIC1/ATP8B1 gene-a novel rare type of mutation associated with benign recurrent intrahepatic cholestasis. [electronic resource] by
- Jirsa, Milan
- Cebecauerova, Dita
- Budisova, Lucie
- Chuzhanova, Nadia
- Hrebicek, Martin
- Dvorakova, Lenka
- Vitek, Libor
- Brodanova, Marie
- Hulek, Petr
- Taimr, Pavel
Publication details: Hepatology research : the official journal of the Japan Society of Hepatology Sep 2004
In:
Hepatology research : the official journal of the Japan Society of Hepatology vol. 30
Availability: No items available.
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