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