TY  -  
T1  - Respiratory chain complex III deficiency due to mutated BCS1L: a novel phenotype with encephalomyopathy, partially phenocopied in a Bcs1l mutant mouse model 
SN  -  /  
UR  - http://hdl.handle.net/10138/180556 
T3  -  
A1  - Tegelberg, Saara; Tomašić, Nikica; Kallijärvi, Jukka; Purhonen, Janne; Elmér, Eskil; Lindberg, Eva; Nord, David G; Soller, Maria; Lesko, Nicole; Wedell, Anna; Bruhn, Helene; Freyer, Christoph; Stranneheim, Henrik; Wibom, Rolf; Nennesmo, Inger; Wredenberg, Anna; Eklund, Erik A; Fellman, Vineta 
A2  -  
PB  - BioMed Central 
Y1  - 2017 
LA  -  
AB  - Abstract
              
                Background
                Mitochondrial diseases due to defective respiratory chain complex III (CIII) are relatively uncommon. The assembly of the eleven-subunit CIII is completed by the insertion of the Rieske iron-sulfur protein, a process for which BCS1L protein is indispensable. Mutations in the BCS1L gene constitute the most common diagnosed cause of CIII deficiency, and the phenotypic spectrum arising from mutations in this gene is wide.
          ... 
VO  -  
IS  -  
SP  -  
OP  -  
KW  - Mitochondrial disorder; Respiratory chain; Respirometry; Assembly factors; Blue native gel electrophoresis; Encephalopathy; Hepatopathy; Microglia; Barrel cortex 
N1  -   
PP  -  
ER  -