Cranioectodermal Dysplasia, Sensenbrenner Syndrome, Is a Ciliopathy Caused by Mutations in the IFT122 Gene
- 1 June 2010
- journal article
- research article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 86 (6) , 949-956
- https://doi.org/10.1016/j.ajhg.2010.04.012
Abstract
No abstract availableKeywords
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