Type I hyperprolinemia (HPI) is an autosomal recessive disorder associated with cognitive and psychiatric troubles, caused by alterations of the Proline Dehydrogenase gene (PRODH) at 22q11. HPI results from PRODH deletion and/or missense mutations reducing proline oxidase (POX) activity. The goals o
✦ LIBER ✦
Physiologic noise obscures genotype–phenotype correlations
✍ Scribed by Richard Kellermayer
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 62 KB
- Volume
- 143A
- Category
- Article
- ISSN
- 1552-4825
No coin nor oath required. For personal study only.
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