QuickView for RARS2;jsessionid=BE3E688A595EC75BA9590A24192A7C9C;jsessionid=3019B5EE2DCD7CF93E24D48A51A7FC0B;jsessionid=B4342EB85148406840B199E869449C3C;jsessionid=71E5997DB084B126BB6369B71CC68EF6;jsessionid=AD0FB4D4804226598797DFF0EE071AD4 (gene)

1. Clinical and genetic analysis of infants with pontocerebellar hypoplasia type 6 caused by RARS2 vari…
2. Expanded clinical phenotype and untargeted metabolomics analysis in RARS2-related mitochondrial diso…
3. Novel RARS2 Variants: Updating the Diagnosis and Pathogenesis of Pontocerebellar Hypoplasia Type 6.
4. Autosomal recessive heterocygote mutation of the RARS2 gene in a colombian patient with non- consang…
5. RARS2 mutations in a sibship with infantile spasms.

There were no clinical trials for RARS2;jsessionid=BE3E688A595EC75BA9590A24192A7C9C;jsessionid=3019B5EE2DCD7CF93E24D48A51A7FC0B;jsessionid=B4342EB85148406840B199E869449C3C;jsessionid=71E5997DB084B126BB6369B71CC68EF6;jsessionid=AD0FB4D4804226598797DFF0EE071AD4