Condition: Progeroid Syndrome, Congenital, Petty Type


rs1553253989 in SLC25A24 gene and Progeroid Syndrome, Congenital, Petty Type PMID 29100093 2017 De Novo Mutations in SLC25A24 Cause a Craniosynostosis Syndrome with Hypertrichosis, Progeroid Appearance, and Mitochondrial Dysfunction.