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RARS2;jsessionid=BE3E688A595EC75BA9590A24192A7C9C
(gene)
Summary
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Parotid gland
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Clinical and genetic analysis of infants with pontocerebellar hypoplasia type 6 caused by RARS2 vari…
Expanded clinical phenotype and untargeted metabolomics analysis in RARS2-related mitochondrial diso…
Novel RARS2 Variants: Updating the Diagnosis and Pathogenesis of Pontocerebellar Hypoplasia Type 6.
Autosomal recessive heterocygote mutation of the RARS2 gene in a colombian patient with non- consang…
RARS2 mutations in a sibship with infantile spasms.
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There were no clinical trials for RARS2;jsessionid=BE3E688A595EC75BA9590A24192A7C9C
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