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Open Access UCL Research: The Interaction of Genetic Mutations in PARK2 and FA2H Causes a Novel Phenotype in a Case of Childhood-Onset Movement Disorder https://t.co/frM3s3Hv3L
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RT @FrontNeurol: New Research: The Interaction of Genetic Mutations in PARK2 and FA2H Causes a Novel Phenotype in a Case of Childhood-Onset…
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RT @FrontNeurol: New Research: The Interaction of Genetic Mutations in PARK2 and FA2H Causes a Novel Phenotype in a Case of Childhood-Onset…
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New Research: The Interaction of Genetic Mutations in PARK2 and FA2H Causes a Novel Phenotype in a Case of Childhood-Onset Movement Disorder: Mutations in the PARK2 gene have been implicated in the pathogenesis of early-onset Parkinson’s… https://t.co/82wt