✦ LIBER ✦
Maternal phenylketonuria syndrome in cousins caused by mild, unrecognized phenylketonuria in their mothers homozygous for the phenylalanine hydroxylase Arg-261-Gln mutation
✍ Scribed by A. Superti-Furga; B. Steinmann; G. Duc; R. Gitzelmann
- Book ID
- 105414098
- Publisher
- Springer
- Year
- 1991
- Tongue
- English
- Weight
- 789 KB
- Volume
- 150
- Category
- Article
- ISSN
- 0340-6997
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