📣 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.

An update on the genetics, clinical presentation, and pathomechanisms of human riboflavin transporter deficiency. (2019)

First Author: O'Callaghan B

Attributed to: Leveraging the power of genomics and transcriptomics to revolutionise the diagnosis and understanding of neurological disorders funded by MRC

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1002/jimd.12053

PubMed Identifier: 30793323

Publication URI: http://europepmc.org/abstract/MED/30793323

Type: Journal Article/Review

Volume: 42

Parent Publication: Journal of inherited metabolic disease

Issue: 4

ISSN: 0141-8955