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Phenylketonuria due to phenylalanine hydroxylase deficiency: an unfolding story
- Source :
- British Medical Journal. January 9, 1993, Vol. 306 Issue 6870, p115, 5 p.
- Publication Year :
- 1993
-
Abstract
- Efficient neonatal screening for phenylketonuria and the availability of complex diets for lifelong use have virtually eliminated severe mental handicap from the disease. Nevertheless, there remains a high risk of [...]
Details
- Language :
- English
- ISSN :
- 17592151
- Volume :
- 306
- Issue :
- 6870
- Database :
- Gale General OneFile
- Journal :
- British Medical Journal
- Publication Type :
- Periodical
- Accession number :
- edsgcl.13383248