QuickView for RARS2;jsessionid=BE3E688A595EC75BA9590A24192A7C9C;jsessionid=3019B5EE2DCD7CF93E24D48A51A7FC0B;jsessionid=672B67699022B99F21945D2FDB5AAF6E;jsessionid=841F7B3FFE77B73274479F6BA6E2B22E (gene)

1. Novel RARS2 Variants: Updating the Diagnosis and Pathogenesis of Pontocerebellar Hypoplasia Type 6.
2. Autosomal recessive heterocygote mutation of the RARS2 gene in a colombian patient with non- consang…
3. RARS2 mutations in a sibship with infantile spasms.
4. A novel mutation in the promoter of RARS2 causes pontocerebellar hypoplasia in two siblings.
5. The bacterial alkyltransferase-like (eATL) protein protects mammalian cells against methylating agen…

There were no clinical trials for RARS2;jsessionid=BE3E688A595EC75BA9590A24192A7C9C;jsessionid=3019B5EE2DCD7CF93E24D48A51A7FC0B;jsessionid=672B67699022B99F21945D2FDB5AAF6E;jsessionid=841F7B3FFE77B73274479F6BA6E2B22E