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Online mutation report
Molecular characterisation of six patients with prolidase deficiency: identification of the first small duplication in the prolidase gene and of a mutation generating symptomatic and asymptomatic outcomes within the same family
- Correspondence to: A Forlino Department of Biochemistry “A Castellani”, Section of Medicine and Pharmacy, University of Pavia, Via Taramelli 3/B, 27100 Pavia, Italy; aforlino{at}unipv.it
Citation
Molecular characterisation of six patients with prolidase deficiency: identification of the first small duplication in the prolidase gene and of a mutation generating symptomatic and asymptomatic outcomes within the same family
Publication history
- Received April 11, 2006
- Accepted June 2, 2006
- Revised May 21, 2006
- First published December 1, 2006.
Online issue publication
December 01, 2006
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Copyright 2006 Journal of Medical Genetics