Brain morphological defects in prolidase deficient mice: first report
<p>Prolidase gene (<em>PEPD</em>) encodes prolidase enzyme, which is responsible for hydrolysis of dipeptides containing proline or hydroxyproline at their C-terminal end. Mutations in <em>PEPD</em> gene cause, in human, prolidase deficiency (PD), a rare autosomal reces...
| Main Authors: | , |
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| Format: | Article |
| Language: | English |
| Published: |
PAGEPress Publications
2014-09-01
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| Series: | European Journal of Histochemistry |
| Subjects: | |
| Online Access: | http://www.ejh.it/index.php/ejh/article/view/2417 |