QuickView for RARS2;jsessionid=BE3E688A595EC75BA9590A24192A7C9C;jsessionid=3019B5EE2DCD7CF93E24D48A51A7FC0B;jsessionid=EB4E8E16473E167B29F5F674D1BC93B9;jsessionid=501CA0B47F62235DAC4D66BEFD1DF8D2;jsessionid=02BDB7C9ADA04C4DD711B18090E0CFB7;jsessionid=9D68439780FE282F183B8C725556E115 (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=EB4E8E16473E167B29F5F674D1BC93B9;jsessionid=501CA0B47F62235DAC4D66BEFD1DF8D2;jsessionid=02BDB7C9ADA04C4DD711B18090E0CFB7;jsessionid=9D68439780FE282F183B8C725556E115