G. Cetta
AuthID: R-00G-E56
1
TITLE: Characterization of a new PEPD allele causing prolidase deficiency in two unrelated patients: natural-occurrent mutations as a tool to investigate structure-function relationship Full Text
AUTHORS: Lupi, A; De Riso, A; Della Torre, S; Rossi, A; Campari, E; Vilarinho, L; Cetta, G; Forlino, A;
PUBLISHED: 2004, SOURCE: JOURNAL OF HUMAN GENETICS, VOLUME: 49, ISSUE: 9
AUTHORS: Lupi, A; De Riso, A; Della Torre, S; Rossi, A; Campari, E; Vilarinho, L; Cetta, G; Forlino, A;
PUBLISHED: 2004, SOURCE: JOURNAL OF HUMAN GENETICS, VOLUME: 49, ISSUE: 9
