Mitochondrial energetic impairment in a patient with late-onset glutaric acidemia Type 2.

Authors

Changrui Xiao
Esteban Astiazaran-Symonds
Shrabani Basu
Monisha Kisling
Fernando Scaglia
Kimberly A. Chapman, George Washington University
Yudong Wang
Jerry Vockley
Carlos R Ferreira

Document Type

Journal Article

Publication Date

10-1-2020

Journal

American Journal of Medical Genetics. Part A

Volume

182

Issue

10

DOI

10.1002/ajmg.a.61786

Keywords

Acyl-CoA Dehydrogenase, Long-Chain; Adult; Age of Onset; Ataxia; Child; Electron-Transferring Flavoproteins; Energy Metabolism; Humans; Iron-Sulfur Proteins; Male; Mitochondria; Mitochondrial Diseases; Multiple Acyl Coenzyme A Dehydrogenase Deficiency; Muscle Weakness; Oxidoreductases Acting on CH-NH Group Donors; Ubiquinone; Young Adult

Comments

Epub 2020 Aug 17

APA Citation

Xiao, C., Astiazaran-Symonds, E., Basu, S., Kisling, M., Scaglia, F., Chapman, K. A., Wang, Y., Vockley, J., & Ferreira, C. (2020). Mitochondrial energetic impairment in a patient with late-onset glutaric acidemia Type 2.. American Journal of Medical Genetics. Part A, 182 (10). http://dx.doi.org/10.1002/ajmg.a.61786

Peer Reviewed

1