Analysis of the Splicing Regulation of the Human Phenylalanine Hydroxylase Gene
碩士 === 國立陽明大學 === 遺傳學研究所 === 92 === Human phenylalanine hydroxylase (PAH) is a liver-specific enzyme, which involved in the rate-limiting step of phenylalanine catabolism. Deficiency of PAH activity results in phenylketonuria, an autosomal recessive disorder. Study has shown that PAH exon 11 s...
| Main Authors: | , |
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| Other Authors: | |
| Format: | Others |
| Language: | zh-TW |
| Published: |
2004
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| Online Access: | http://ndltd.ncl.edu.tw/handle/10419317587709550196 |