Missing/wrong data?
Log in to edit
Cranioectodermal Dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 gene
scientific article
Author/s
author: Andreas Tzschach, Hans-Hilger Ropers, Jacek Zachwieja, Daniel Osborn, Masoud Garshasbi, Anna Latos-Bieleńska, Danuta Zwolińska, Joanna Walczak-Sztulpa, Francesco Emma
Work details
Publication date
June 11, 2010
-
-
Language
English
Copyright status
Copyright status information is not available for this work. The copyright status depends on the jurisdiction, the author's date of death and the date the work was created or published.
To learn more about copyright terms in different countries, visit the countries and terms page.