Respiratory chain complex III deficiency due to mutated BCS1L: a novel phenotype with encephalomyopathy, partially phenocopied in a Bcs1l mutant mouse model
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V. Fellman | E. Eklund | J. Kallijärvi | E. Elmér | R. Wibom | Janne Purhonen | H. Stranneheim | C. Freyer | A. Wredenberg | M. Soller | I. Nennesmo | A. Wedell | E. Lindberg | S. Tegelberg | D. G. Nord | Nicole Lesko | N. Tomasic | Helene Bruhn | J. Purhonen | Saara Tegelberg | Christoph Freyer | Nikica Tomašić