Succinate-CoA Ligase: Difference between revisions
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Succinate-CoA ligase is associated with the syndrome autosomal recessive mitochondrial DNA depletion syndrome-9. Patients with this syndrome can have a variable degree of phenotypes depending on which mutated gene | Succinate-CoA ligase is associated with the syndrome [[autosomal recessive mitochondrial DNA depletion syndrome-9|autosomal recessive mitochondrial DNA depletion syndrome-9]]. Patients with this syndrome can have a variable degree of [[phenotypes|phenotypes]] depending on which mutated [[genes|gene]]<ref>Ostergaard, E., Christensen, E., Kristensen, E., Mogensen, B., Duno, M., Shoubridge, E. A., Wibrand, F. Deficiency of the alpha subunit of succinate-coenzyme A ligase causes fatal infantile lactic acidosis with mitochondrial DNA depletion. Am. J. Hum. Genet. 81: 383-387, 2007</ref>. | ||
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Latest revision as of 10:02, 20 October 2016
Succinate-CoA ligase is associated with the syndrome autosomal recessive mitochondrial DNA depletion syndrome-9. Patients with this syndrome can have a variable degree of phenotypes depending on which mutated gene[1].
References
- ↑ Ostergaard, E., Christensen, E., Kristensen, E., Mogensen, B., Duno, M., Shoubridge, E. A., Wibrand, F. Deficiency of the alpha subunit of succinate-coenzyme A ligase causes fatal infantile lactic acidosis with mitochondrial DNA depletion. Am. J. Hum. Genet. 81: 383-387, 2007