Respiratory chain complex III deficiency due to mutated BCS1L: a novel phenotype with encephalomyopathy, partially phenocopied in a Bcs1l mutant mouse model

Overview of attention for article published in Orphanet Journal of Rare Diseases, April 2017

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RT @varsome: BCS1L #mutations https://t.co/Letl2qGJuy cause encephalomyopathy #respiratory chain complex III deficiency #Genetics https://t…

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BCS1L #mutations https://t.co/Letl2qGJuy cause encephalomyopathy #respiratory chain complex III deficiency #Genetics https://t.co/7FLQNIfUXj

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Another one out! from #gracilelab at #folkhalsan in #ojrarediseases Funded by #suomenakatemia #vetenskapsradet https://t.co/Xb23XLkJ6A

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