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

First Author: O'Callaghan B

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