Maternal riboflavin deficiency, resulting in transient neonatal-onset glutaric aciduria Type 2, is caused by a microdeletion in the riboflavin transporter gene GPR172BGladys Ho, John Christodoulou, Rikke Katrine Jentoft Olsen et al.|Human Mutation|2010Cited by 120
Transient multiple acyl-CoA dehydrogenation deficiency in a newborn female caused by maternal riboflavin deficiencyMary Anne D. Chiong, John Christodoulou, Keow Giak Sim et al.|Molecular Genetics and Metabolism|2007Cited by 49
Maternal riboflavin deficiency,resulting in transient neonatal-onset glutaric aciduria Type 2, is caused by amicrodeletion in the riboflavin transporter gene GPR172BGladys Ho, John Christodoulou, Gregory B. Peters et al.|Unknown|2011Cited by 0