A Missense Mutation (R565W) in Cirhin (FLJ14728) in North American Indian Childhood Cirrhosis

Study concludes that a single gene mutation causes North American Indian Childhood Cirrhosis, a distinct and severe form of familial cholestasis, which occurs in aboriginal children in the Abitibi region of northwestern Quebec.
Author/Creator
Pierre Chagnon
Jacques Michaud
Grant Mitchell
Jocelyne Mercier
Marion Jean-Francois
et al.
Open Access
No
Primary Source
No
Citation
American Journal of Human Genetics, vol. 71, no. 6, December 2002, pp. 1443-1449
Publication Date
2002-12
Location
Resource Type
Articles -- Scholarly, peer reviewed
Format
Text -- PDF
Text -- HTML
Language
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