Complex inheritance of familial hypercholanemia with associated mutations in TJP2 and BAAT.
Autor: | Carlton, Victoria E. H., Harris, Baruch Z., Puffenberger, Erik G., Batta, A. K., Knisely, A. S., Robinson, Donna L., Strauss, Kevin A., Shneider, Benjamin L., Lim, Wendell A., Salen, Gerald, Morton, D Holmes, Bull, Laura N. |
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Zdroj: | Nature Genetics. May2003, Vol. 34 Issue 1, p91. 6p. |
Databáze: | Academic Search Ultimate |
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