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 |
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Zdroj: | European Journal of Human Genetics. Jun2013, Vol. 21 Issue 6, p691-694. 4p. 1 Diagram, 2 Charts. |
Databáze: | Academic Search Ultimate |
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