Phenylketonuria (PKU) is an autosomal recessive disorder caused by a deficiency of the phenylalanine hydroxylation system and is characterized by a block in the conversion of phenylalanine (PHE) to tyrosine. We examined the effects of maternal hyperphenylalaninemia on the morphological and biochemic
Adaptations to oxidative stress induced by vitamin E deficiency in rat liver
β Scribed by Rafael de Cabo; John R. Burgess; Placido Navas
- Publisher
- Springer US
- Year
- 2006
- Tongue
- English
- Weight
- 305 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0145-479X
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