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Characterization of complex III deficiency and liver dysfunction in GRACILE syndrome caused by a BCS1L mutation

(2010) MITOCHONDRION. 10(5). p.497-509
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Keywords
MITOCHONDRIAL RESPIRATORY-CHAIN, Fellman syndrome, FETAL-GROWTH-RETARDATION, HYPOXIA-INDUCIBLE FACTOR, POLYACRYLAMIDE-GEL ELECTROPHORESIS, BLUE-NATIVE-ELECTROPHORESIS, LETHAL METABOLIC-DISORDER, CYTOCHROME BC(1) COMPLEX, OXIDATIVE-PHOSPHORYLATION, LACTIC-ACIDOSIS, IRON-OVERLOAD, Ceruloplasmin, Hemochromatosis, Core I, Rieske FeS protein, Mitochondria

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Citation

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Chicago
Kotarsky, Heike, Riitta Karikoski, Matthias Morgelin, Sanna Marjavaara, Petra Bergman, De-Liang Zhang, Joél Smet, Rudy Van Coster, and Vineta Fellman. 2010. “Characterization of Complex III Deficiency and Liver Dysfunction in GRACILE Syndrome Caused by a BCS1L Mutation.” Mitochondrion 10 (5): 497–509.
APA
Kotarsky, H., Karikoski, R., Morgelin, M., Marjavaara, S., Bergman, P., Zhang, D.-L., Smet, J., et al. (2010). Characterization of complex III deficiency and liver dysfunction in GRACILE syndrome caused by a BCS1L mutation. MITOCHONDRION, 10(5), 497–509.
Vancouver
1.
Kotarsky H, Karikoski R, Morgelin M, Marjavaara S, Bergman P, Zhang D-L, et al. Characterization of complex III deficiency and liver dysfunction in GRACILE syndrome caused by a BCS1L mutation. MITOCHONDRION. 2010;10(5):497–509.
MLA
Kotarsky, Heike, Riitta Karikoski, Matthias Morgelin, et al. “Characterization of Complex III Deficiency and Liver Dysfunction in GRACILE Syndrome Caused by a BCS1L Mutation.” MITOCHONDRION 10.5 (2010): 497–509. Print.
@article{1060719,
  author       = {Kotarsky, Heike and Karikoski, Riitta and Morgelin, Matthias and Marjavaara, Sanna and Bergman, Petra and Zhang, De-Liang and Smet, Joél and Van Coster, Rudy and Fellman, Vineta},
  issn         = {1567-7249},
  journal      = {MITOCHONDRION},
  keywords     = {MITOCHONDRIAL RESPIRATORY-CHAIN,Fellman syndrome,FETAL-GROWTH-RETARDATION,HYPOXIA-INDUCIBLE FACTOR,POLYACRYLAMIDE-GEL ELECTROPHORESIS,BLUE-NATIVE-ELECTROPHORESIS,LETHAL METABOLIC-DISORDER,CYTOCHROME BC(1) COMPLEX,OXIDATIVE-PHOSPHORYLATION,LACTIC-ACIDOSIS,IRON-OVERLOAD,Ceruloplasmin,Hemochromatosis,Core I,Rieske FeS protein,Mitochondria},
  language     = {eng},
  number       = {5},
  pages        = {497--509},
  title        = {Characterization of complex III deficiency and liver dysfunction in GRACILE syndrome caused by a BCS1L mutation},
  url          = {http://dx.doi.org/10.1016/j.mito.2010.05.009},
  volume       = {10},
  year         = {2010},
}

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