| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 8390757 | Molecular Genetics and Metabolism Reports | 2016 | 4 Pages |
Abstract
In conclusion, these were the first genetically confirmed cases of PKU in Mongolia, and the study suggested that the newborn screening program for PKU was significant because it enabled early treatment dietary restriction, specialized formulas and other medical management for prevention of neurological handicaps in these children.
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Authors
Jamiyan Purevsuren, Baasandai Bolormaa, Chogdon Narantsetseg, Renchindorj Batsolongo, Ochirbat Enkhchimeg, Munkhuu Bayalag, Yuki Hasegawa, Haruo Shintaku, SeijiYamaguchi SeijiYamaguchi,