Brain morphological defects in prolidase deficient mice: first report

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...

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Bibliographic Details
Main Authors: V. Insolia, V.M. Piccolini
Format: Article
Language:English
Published: PAGEPress Publications 2014-09-01
Series:European Journal of Histochemistry
Subjects:
Mental retardation
prolidase deficiency
postnatal development
CNS alteration
cardiac hypertrophy
extracellular matrix.
Online Access:http://www.ejh.it/index.php/ejh/article/view/2417

Internet

http://www.ejh.it/index.php/ejh/article/view/2417

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