Mutations in C5ORF42 Cause Joubert Syndrome in the French Canadian Population
Open Access
- 15 March 2012
- journal article
- other
- Published by Elsevier in American Journal of Human Genetics
- Vol. 90 (4), 693-700
- https://doi.org/10.1016/j.ajhg.2012.02.011
Abstract
No abstract availableKeywords
This publication has 35 references indexed in Scilit:
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