Investigating neurological deficits in carriers and affected patients with ornithine transcarbamylase deficiency.

Authors

Courtney Sprouse
Jessica King
Guy HelmanFollow
Ileana Pacheco-Colón
Kyle Shattuck
Andrew Breeden
Rebecca Seltzer
John W. VanMeter
Andrea L. Gropman, George Washington University

Document Type

Journal Article

Publication Date

9-2014

Journal

Molecular Genetics and Metabolism

Volume

Volume 113, Issue 1-2

Issue

1-2

Inclusive Pages

136-141

Keywords

Cognition Disorders--etiology; Cognition Disorders--physiopathology; Heterozygote; Ornithine Carbamoyltransferase Deficiency Disease--complications; Ornithine Carbamoyltransferase Deficiency Disease--genetics

APA Citation

Sprouse, C., King, J., Helman, G., Pacheco-Colon, I., Shattuck, K. et al. (2014). Investigating neurological deficits in carriers and affected patients with ornithine transcarbamylase deficiency. Molecular Genetics and Metabolism, 113(1-2), 136-141.

Peer Reviewed

1