Mitochondrial Myopathy Due to Complex III Deficiency with Normal Reducible Cytochrome B Concentration
Overview
Affiliations
Mitochondrial DNA mutations in multiple symmetric lipomatosis.
Klopstock T, Naumann M, Seibel P, Shalke B, Reiners K, Reichmann H Mol Cell Biochem. 1997; 174(1-2):271-5.
PMID: 9309699
Progression of myopathology in Kearns-Sayre syndrome: a morphological follow-up study.
Reichmann H, Gold R, Meurers B, Naumann M, Seibel P, Walter U Acta Neuropathol. 1993; 85(6):679-81.
PMID: 8393264 DOI: 10.1007/BF00334681.
3.1-kb deletion of mitochondrial DNA in a patient with Kearns-Sayre syndrome.
Klopstock T, Bischof F, Gerok K, Deuschl G, Seibel P, Ketelsen U Acta Neuropathol. 1995; 90(2):126-9.
PMID: 7484086 DOI: 10.1007/BF00294310.
The biochemical basis of mitochondrial diseases.
Scholte H J Bioenerg Biomembr. 1988; 20(2):161-91.
PMID: 3286631 DOI: 10.1007/BF00768393.
Variability in the activity of respiratory chain enzymes in mitochondrial myopathies.
Koga Y, Nonaka I, Sunohara N, Yamanaka R, Kumagai K Acta Neuropathol. 1988; 76(2):135-41.
PMID: 2841822 DOI: 10.1007/BF00688097.