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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| Description | scientific article |
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author: Janne Purhonen Anna Wredenberg Christoph Freyer Jukka Kallijarvi Saara Tegelberg |
| Publication date | April 20, 2017 |
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