Impairment of cognitive function in ornithine transcarbamylase deficiency is global rather than domain-specific and is associated with disease onset, sex, maximum ammonium, and number of hyperammonemic events.

Authors

Corinna Buerger
Sven F Garbade
Fabienne Dietrich Alber
Susan E Waisbren
Robert McCarter, George Washington University
Stefan Kölker
Peter Burgard

Document Type

Journal Article

Publication Date

12-27-2018

Journal

Journal of inherited metabolic disease

DOI

10.1002/jimd.12013

Comments

Epub ahead of print

APA Citation

Buerger, C., Garbade, S., Dietrich Alber, F., Waisbren, S., McCarter, R., Kölker, S., & Burgard, P. (2018). Impairment of cognitive function in ornithine transcarbamylase deficiency is global rather than domain-specific and is associated with disease onset, sex, maximum ammonium, and number of hyperammonemic events.. Journal of inherited metabolic disease, (). http://dx.doi.org/10.1002/jimd.12013

Peer Reviewed

1