Phenotypic analysis of epilepsy in the mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes-associated mitochondrial DNA A3243G mutation

Authors

Scott T. Demarest, Children's National Medical CenterFollow
Matthew T. Whitehead, Children's National Medical CenterFollow
Sinan Turnacioglu, George Washington University
Phillip L. Pearl, George Washington UniversityFollow
Andrea L. Gropman, George Washington University

Document Type

Journal Article

Publication Date

2014

Journal

Journal of Child Neurology

Volume

Volume 29, Issue 9

Inclusive Pages

1249-1256

Keywords

Brain--physiopathology; DNA, Mitochondrial; Epilepsy--genetics; Epilepsy--physiopathology; MELAS Syndrome--genetics; MELAS Syndrome--physiopathology

APA Citation

Demarest, S. T., Whitehead, M. T., Turnacioglu, S., Pearl, P. L., & Gropman, A. L. (2014). Phenotypic analysis of epilepsy in the mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes-associated mitochondrial DNA A3243G mutation. Journal of Child Neurology, 29(9), 1249-1256.

Peer Reviewed

1