Phenylalanine hydroxylase mRNA rescues the phenylketonuria phenotype in mice
Phenylketonuria (PKU) is an inborn error of metabolism caused by a deficiency in functional phenylalanine hydroxylase (PAH), resulting in accumulation of phenylalanine (Phe) in patients’ blood and organs. Affected patients encounter severe developmental delay, neurological deficits, and behavioral a...
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| Asıl Yazarlar: | , , , , , , , , , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Frontiers Media S.A.
2022-10-01
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| Seri Bilgileri: | Frontiers in Bioengineering and Biotechnology |
| Konular: | |
| Online Erişim: | https://www.frontiersin.org/articles/10.3389/fbioe.2022.993298/full |
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