Respiratory Chain Complex III Deficiency Due to Mutated BCS1L: A Novel Phenotype With Encephalomyopathy, Partially Phenocopied in a Bcs1l Mutant Mouse Model
Orphanet Journal of Rare Diseases - United Kingdom
doi 10.1186/s13023-017-0624-2
Full Text
Open PDFAbstract
Available in full text
Date
April 20, 2017
Authors
Publisher
Springer Science and Business Media LLC