Case Report: Rare Homozygous RNASEH1 Mutations Associated With Adult-Onset Mitochondrial Encephalomyopathy and Multiple Mitochondrial DNA Deletions
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G. Comi | S. Corti | V. Carelli | A. Toscano | S. Zanotti | L. Caporali | O. Musumeci | D. Piga | M. Meneri | D. Ronchi | I. Arena | Arianna Manini