Coenzyme Q10 Deficiency and Type 2C Muscle Fibers
Abstract
Investigators at Washington University School of Medicine, St Louis, MO, evaluated retrospectively clinical, laboratory, and muscle histochemistry and oxidative enzyme characteristics in 49 children with suspected mitochondrial disorders.
DOI: https://doi.org/10.15844/pedneurbriefs-27-12-9 | Journal eISSN: 2166-6482
Language: English
Page range: 96 - 96
Published on: Dec 1, 2013
Published by: Pediatric Neurology Briefs Publishers
In partnership with: Paradigm Publishing Services
© 2013 J Gordon Millichap, published by Pediatric Neurology Briefs Publishers
This work is licensed under the Creative Commons Attribution 4.0 License.