Mutations in the human phenylalanine hydroxylase gene producing phenylketonuria or hyperphenylalaninemia have now been identified in many patients from various ethnic groups. These mutations all exhibit a high degree of association with specific restriction fragment-length polymorphism haplotypes at
✦ LIBER ✦
Preliminary studies on the molecular basis of hyperphenylalaninemia in Egypt
✍ Scribed by Nemat Hashem; Paolo Bosco; Valeria Chiavetta; Francesco Calì; Nadia Ceratto; V. Romano
- Publisher
- Springer
- Year
- 1996
- Tongue
- English
- Weight
- 51 KB
- Volume
- 98
- Category
- Article
- ISSN
- 0340-6717
No coin nor oath required. For personal study only.
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