Results
Title

Maternal riboflavin deficiency, resulting in transient neonatal-onset glutaric aciduria Type 2, is caused by a microdeletion in the riboflavin transporter gene GPR172B.

Authors

Ho, Gladys; Yonezawa, Atsushi; Masuda, Satohiro; Inui, Ken-ichi; Sim, Keow G.; Carpenter, Kevin; Olsen, Rikke K.J.; Mitchell, John J.; Rhead, William J.; Peters, Gregory; Christodoulou, John

Publication

Human Mutation, 2011, Vol 32, Issue 1, pE1976

ISSN

1059-7794

Publication type

Academic Journal

DOI

10.1002/humu.21399