CLCA4 variants determine the manifestation of the cystic fibrosis basic defect in the intestine.

Autor: Kolbe, Ernst-Wolfgang1, Tamm, Stephanie1, Hedtfeld, Silke1, Becker, Tim2, Tümmler, Burkhard3, Stanke, Frauke3
Zdroj: European Journal of Human Genetics. Jun2013, Vol. 21 Issue 6, p691-694. 4p. 1 Diagram, 2 Charts.
Databáze: Academic Search Ultimate