Respiratory chain complex III deficiency due to mutated BCS1L: a novel phenotype with encephalomyopathy, partially phenocopied in a Bcs1l mutant mouse modelSaara Tegelberg(Lund University), Vineta Fellman(University of Helsinki)Orphanet Journal of Rare DiseasesApril 20, 201710.1186/s13023-017-0624-2Cited by 32SaveCiteExport RISWatch citationsRelated PapersNAD <sup>+</sup> repletion produces no therapeutic effect in mice with respiratory chain complex III deficiency and chronic energy deprivation|The FASEB Journal|2018|22