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Another "Complex" Case: Complex I Deficiency Secondary to Acyl-CoA Dehydrogenase 9 Mutation.
- Source :
-
The American journal of the medical sciences [Am J Med Sci] 2015 Nov; Vol. 350 (5), pp. 423-4. - Publication Year :
- 2015
- Subjects :
- Adolescent
Diet Therapy methods
Disease Management
Humans
Male
Mutation, Missense
Secondary Prevention
Ubiquinone administration & dosage
Vitamins administration & dosage
Acyl-CoA Dehydrogenases genetics
Mitochondrial Myopathies congenital
Mitochondrial Myopathies diagnosis
Mitochondrial Myopathies physiopathology
Mitochondrial Myopathies therapy
Rhabdomyolysis blood
Rhabdomyolysis etiology
Rhabdomyolysis physiopathology
Rhabdomyolysis prevention & control
Riboflavin administration & dosage
Ubiquinone analogs & derivatives
Subjects
Details
- Language :
- English
- ISSN :
- 1538-2990
- Volume :
- 350
- Issue :
- 5
- Database :
- MEDLINE
- Journal :
- The American journal of the medical sciences
- Publication Type :
- Academic Journal
- Accession number :
- 26445304
- Full Text :
- https://doi.org/10.1097/MAJ.0000000000000570