| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 8390445 | Molecular Genetics and Metabolism Reports | 2018 | 5 Pages |
Abstract
In the light of the results obtained, we will continue to screen the congenital acquired vitamin B12 deficiency among our NBS program. Every child with aberrant C3, C3/C2 and C3/C16 will be thoroughly examined to exclude acquired vitamin B12 deficiency, which can easily be corrected in most cases.
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Authors
Karit Reinson, Kadi Künnapas, Annika Kriisa, Mari-Anne Vals, Kai Muru, Katrin Ãunap,