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

Authors

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

Document Type

Journal Article

Publication Date

9-1-2014

Journal

Molecular Genetics and Metabolism

Volume

Volume 113, Issue 1

Inclusive Pages

136-141

Keywords

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

Comments

PMCID: PMC4458385 [Available on 2015-09-01]

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), 136-141.

Peer Reviewed

1