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Phenylketonuria screening in the Republic of Macedonia
Phenylketonuria is an autosomal recessive inborn error of metabolism which can be prevented by early and continuous treatment. Therefore newborn screening for phenylketonuria has been introduced in many countries. We present here the results of the selective newborn screening for inborn errors of me...
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| Udgivet i: | Orphanet J Rare Dis |
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| Main Authors: | , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
BioMed Central
2016
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4975894/ https://ncbi.nlm.nih.gov/pubmed/27496147 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13023-016-0483-2 |
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