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Peak bone mass in patients with phenylketonuria

✍ Scribed by D. Modan-Moses; I. Vered; G. Schwartz; Y. Anikster; S. Abraham; R. Segev; Ori Efrati


Publisher
Springer
Year
2007
Tongue
English
Weight
253 KB
Volume
30
Category
Article
ISSN
0141-8955

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During routine screening procedures for amino-acid disorders by thin-layer chromatography, a 16-year-old boy was found to have phenylketonuria and cystinuria. A phenylalanine and a cystine loading were carried out. The patient was found to be homozygous for phenylketonuria and heterozygous for cysti