Phenylketonuria and other phenylalanine hydroxylation mutants in man. [electronic resource]
Producer: 19810526Description: 179-202 p. digitalISSN:- 0066-4197
- Alleles
- Amino Acid Metabolism, Inborn Errors -- diagnosis
- Animals
- Biopterins -- analogs & derivatives
- Dihydropteridine Reductase -- genetics
- Female
- Fetal Diseases -- etiology
- Gene Frequency
- Genetic Carrier Screening
- Heterozygote
- Humans
- Hydroxylation
- Phenylalanine -- metabolism
- Phenylalanine Hydroxylase -- deficiency
- Phenylketonurias -- diet therapy
- Pregnancy
- Pregnancy Complications
- Rats
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Review
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