Cranioectodermal Dysplasia, Sensenbrenner syndrome, is a ciliopathy caused by mutations in the IFT122 gene
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| Description | scientific article |
| Author/s |
author: Hans-Hilger Ropers Andreas Tzschach Masoud Garshasbi Daniel Osborn Francesco Emma Joanna Walczak-Sztulpa Danuta Zwolińska Anna Latos-Bieleńska Jacek Zachwieja |
| Publication date | June 11, 2010 |
| Language | English |
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