Novel homozygous RARS2 mutation in two siblings without pontocerebellar hypoplasia – further expansion of the phenotypic spectrum

Overview of attention for article published in Orphanet Journal of Rare Diseases, October 2016

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Novel homozygous RARS2 mutation in two siblings without pontocerebellar hypoplasia – further expansion of the... https://t.co/rEqMr6h0N7

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RT @ojrarediseases: Mutation in two siblings without pontocerebellar hypoplasia #OJRD #RareDisease #PontocerebellarHypoplasia https://t.co/…

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Mutation in two siblings without pontocerebellar hypoplasia #OJRD #RareDisease #PontocerebellarHypoplasia https://t.co/VHwFD3oMJT

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