Myopathic mitochondrial DNA depletion syndrome associated with biallelic variants in LIG3

BMBF10.13039/50110000234701GM1920AItalian MoHJ42F19000030006-RE17Horizon 202010.13039/100010661N °825575European Joint Programme on Rare DiseasesBMBF10.13039/50110000234701KU2016AItalian MoHJ49C2000019000-RE15ERA PerMed project PerMiMGerman Network for Mitochondrial Disorders01GM1906DCenter for the Study of Mitochondrial Pediatric Diseases fundedLuisa Mariani Foundation
Source: Brain - Category: Neurology Source Type: research