QuickView for NR_146741 (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 NR_146741