📣 Help Shape the Future of UKRI's Gateway to Research (GtR)

We're improving UKRI's Gateway to Research and are seeking your input! If you would be interested in being interviewed about the improvements we're making and to have your say about how we can make GtR more user-friendly, impactful, and effective for the Research and Innovation community, please email gateway@ukri.org.

Neurocognitive outcome and mental health in children with tyrosinemia type 1 and phenylketonuria: A comparison between two genetic disorders affecting the same metabolic pathway. (2022)

First Author: Van Vliet K

Attributed to: Development of rAAV-mediated gene therapy for a severe paediatric metabolic liver disease: Ornithine Transcarbamylase deficiency. funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1002/jimd.12528

PubMed Identifier: 35722880

Publication URI: http://europepmc.org/abstract/MED/35722880

Type: Journal Article/Review

Volume: 45

Parent Publication: Journal of inherited metabolic disease

Issue: 5

ISSN: 0141-8955