Extraction of phenylalanine ammonia lyase from Anabaena variabilis isolates from Iran
Phenylketonuria is an autosomal genetic disorder characterized by a deficiency of phenylalanine hydroxylase, leading to the accumulation of phenylalanine in the blood instead of its metabolism and excretion. This accumulation can result in intellectual disabilities in infants. Phenylalanine ammonia...
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| Hlavní autoři: | , , , , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Taylor & Francis Group
2025-12-01
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| Edice: | Applied Phycology |
| Témata: | |
| On-line přístup: | https://www.tandfonline.com/doi/10.1080/26388081.2025.2536292 |
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