Characterization of a new PEPD allele causing prolidase deficiency in two unrelated patients: natural-occurrent mutations as a tool to investigate structure-function relationship (Q28277017)

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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
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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 (English)
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    Anna Lupi
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    Antonio De Riso
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    Sara Della Torre
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    Antonio Rossi
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    Elena Campari
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    Laura Vilarinho
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    Giuseppe Cetta
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    Antonella Forlino
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    2004
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    49
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    500-6
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    9
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