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Mutation analysis of Phenylalanine hydroxylase gene in Iranian patients with Phenylketonuria
Background: Phenylketonuria as the most common genetic metabolic disorder is the result of disruption of the phenylalanine hydroxylase gene. This study was carried out to explore the phenylalanine hydroxylase gene mutation status of Iranian phenylketonuria patients. Methods: Blood samples were colle...
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| Vydáno v: | Med J Islam Repub Iran |
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| Hlavní autoři: | , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Iran University of Medical Sciences
2018
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6108261/ https://ncbi.nlm.nih.gov/pubmed/30159272 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.14196/mjiri.32.21 |
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