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
β¦ LIBER β¦
Prevention of Allylisopropylacetamide Induced Experimental Porphyria in the Rat by Vitamin E
β Scribed by MURTY, HARI S.; NAIR, PADMANABHAN P.
- Book ID
- 109668281
- Publisher
- Nature Publishing Group
- Year
- 1969
- Tongue
- English
- Weight
- 236 KB
- Volume
- 223
- Category
- Article
- ISSN
- 0028-0836
- DOI
- 10.1038/223200a0
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