A novel missense mutation in SUCLG1 associated with mitochondrial DNA depletion, encephalomyopathic form, with methylmalonic aciduria

Overview of attention for article published in European Journal of Pediatrics, June 2009

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TREATMENT OF MITOCHONDRIAL DISEASES

Application EP-4218938-A1

European Patent Office

TREATMENT OF MITOCHONDRIAL DISEASES

Application WO-2016193421-A1

World Intellectual Property Organisation (WIPO)