Maternal riboflavin deficiency, resulting in transient neonatal-onset glutaric aciduria Type 2, is caused by a microdeletion in the riboflavin transporter gene GPR172B. (Q51532162)
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scientific article published in January 2011
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Maternal riboflavin deficiency, resulting in transient neonatal-onset glutaric aciduria Type 2, is caused by a microdeletion in the riboflavin transporter gene GPR172B. |
scientific article published in January 2011 |
Statements
Maternal riboflavin deficiency, resulting in transient neonatal-onset glutaric aciduria Type 2, is caused by a microdeletion in the riboflavin transporter gene GPR172B (English)
Gladys Ho
Satohiro Masuda
Ken-ichi Inui
Keow G Sim
Kevin Carpenter
William J Rhead