De Novo Mutations in SLC25A24 Cause a Craniosynostosis Syndrome with Hypertrichosis, Progeroid Appearance, and Mitochondrial Dysfunction
Open Access
- 1 November 2017
- journal article
- other
- Published by Elsevier BV in American Journal of Human Genetics
- Vol. 101 (5), 833-843
- https://doi.org/10.1016/j.ajhg.2017.09.016
Abstract
No abstract availableKeywords
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