Phenylketonuria: Difference between revisions
Jump to navigation
Jump to search
m Created page with " This is a disorder caused by the deficiency of phenylalanine hydroxylase hence the patient is unable to digest phenylalanine<ref>. Stryer,L., Jeremy M. Berg and John L. Ty..." |
No edit summary |
||
| Line 1: | Line 1: | ||
This is a disorder caused by the deficiency of phenylalanine hydroxylase hence the patient is unable to digest phenylalanine<ref>. Stryer,L., Jeremy M. Berg and John L. Tymoczko Biochemistry, 5th Ed.</ref>. | This is a disorder caused by the deficiency of [[phenylalanine hydroxylase|phenylalanine hydroxylase]] hence the patient is unable to digest [[Phenylalanine|phenylalanine]] <ref>. Stryer,L., Jeremy M. Berg and John L. Tymoczko Biochemistry, 5th Ed.</ref>. | ||
=== References === | |||
<references /> | <references /> | ||
Revision as of 10:11, 12 November 2011
This is a disorder caused by the deficiency of phenylalanine hydroxylase hence the patient is unable to digest phenylalanine [1].
References
- ↑ . Stryer,L., Jeremy M. Berg and John L. Tymoczko Biochemistry, 5th Ed.