Maternal riboflavin deficiency, resulting in transient neonatal-onset glutaric aciduria Type 2, is caused by a microdeletion in the riboflavin transporter gene GPR172B.
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| Description | scientific article published in January 2011 |
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author: John J. Mitchell Rikke K. Olsen Atsushi Yonezawa John Christodoulou |
| Publication date | January 1, 2011 |
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