Works by Sim, Keow G.

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

Published in:

Human Mutation, 2011, v. 32, n. 1, p. E1976, doi. 10.1002/humu.21399

By:

• 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 type:

Article