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

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

DOI Full Paper Access

32

Citations

24

References

2017

Year

Saara Tegelberg, Nikica Tomašić, Jukka Kallijärvi, Janne Purhonen, Eskil Elmér, Eva Hellström Lindberg, D. Nord, Maria Soller, Nicole Lesko, Anna Wedell,

Orphanet Journal of Rare Diseases

References

	Year	Citations

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