Molecular Genetic Study of a Novel Phenylketonuria Mutation
碩士 === 國立陽明大學 === 遺傳學研究所 === 87 === Phenylketouria (PKU, MIM 261600) is a human genetic disorder resulting from deficiency of phenylalanine hydroxylation system in liver. Early diagnosis of PKU, a cause of mental retardation, is important because the mental retardation can be prevented by...
| Main Authors: | , |
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| Format: | Others |
| Language: | zh-TW |
| Published: |
1999
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| Online Access: | http://ndltd.ncl.edu.tw/handle/03911364528967432379 |