Published in
Wiley, Journal of Inherited Metabolic Disease, 4(42), p. 598-607, 2019
DOI: 10.1002/jimd.12053
Links
Tools
An update on the genetics, clinical presentation, and pathomechanisms of human riboflavin transporter deficiency
This paper was not found in any repository, but could be made available legally by the author.
Full text: Unavailable
Published version:
archiving forbidden
Data provided by 