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.
Zdroj: Nature Genetics. May2003, Vol. 34 Issue 1, p91. 6p.
Databáze: Academic Search Ultimate