Analog kefir production with a low phenylalanine for Phenylketonuria
Phenylketonuria (PKU) is one of the most prevalent types of hereditary metabolic disorders which is caused due to an absence or reduction of the activity of the Phenylalanine hydroxylase enzyme in the liver which in turn, inhibits the transformation of phenylalanine (Phe) to tyrosine. In clinical te...
| Main Authors: | , |
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| Format: | Article |
| Language: | English |
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Islamic Azad University
2017-06-01
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| Series: | Journal of Pharmaceutical and Health Sciences |
| Subjects: | |
| Online Access: | http://www.jphs.ir/article_529345.html |