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.