Rett Syndrome and Mitochondrial Enzyme Deficiencies
DOI:
https://doi.org/10.15844/pedneurbriefs-5-5-13Keywords:
Muscle Mitochondrial, Clonic Seizures, Succinate CytochromeAbstract
Three children with Rett syndrome and normal muscle mitochondrial structure but abnormalities in mitochondrial respiratory chain enzymes are reported from the Departments of Neurology and Pediatrics, Loyola University, Stritch School of Medicine, Maywood, IL.Published
1991-05-01
Issue
Section
Rett Syndrome
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Copyright (c) 1991 The Author(s)
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