Maternal riboflavin deficiency, resulting in transient neonatal-onset glutaric aciduria Type 2, is caused by a microdeletion in the riboflavin transporter gene GPR172B
Gladys Ho(The University of Sydney), John Christodoulou(The University of Melbourne), Atsushi Yonezawa(Kyoto University Hospital), Rikke Katrine Jentoft Olsen(Aarhus University Hospital), Keow Giak Sim(Children's Hospital at Westmead), Gregory B. Peters(Children's Hospital at Westmead), Ken‐ichi Inui(Kyoto Pharmaceutical University), John J. Mitchell(University of North Carolina at Chapel Hill), William J. Rhead(Children's Hospital of Wisconsin), Kevin Carpenter(The University of Sydney), Satohiro Masuda(Himeji Dokkyo University)
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