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Characterization of a new PEPD allele causing prolidase deficiency in two unrelated patients: natural-occurrent mutations as a tool to investigate structure–function relationship
Anna Lupi, Antonio De Riso, Sara Della Torre, Antonio Rossi, Elena Campari, Laura Vilarinho, Giuseppe Cetta, Antonella ForlinoVolume:
49
Language:
english
Pages:
7
DOI:
10.1007/s10038-004-0180-1
Date:
September, 2004
File:
PDF, 1.55 MB
english, 2004