Characterization of a New Pepd Allele Causing Prolidase Deficiency in Two Unrelated Patients: Natural-Occurrent Mutations as a Tool to Investigate Structure-Function Relationship

AuthID
 P-000-D26
8
Author(s)
Lupi, A
·
Della Torre, S
·
Rossi, A
·
Campari, E
·
Forlino, A
Tipo de Documento
Article
Year published
2004
Publicado
in JOURNAL OF HUMAN GENETICS, ISSN: 1435-232X
Volume: 49, Número: 9, Páginas: 500-506 (7)
Indexing
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Scopus®
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Pubmed®
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Publication Identifiers
Pubmed: 15309682
SCOPUS: 2-s2.0-4744341131
Wos: WOS:000224055000007
Source Identifiers
ISSN: 1435-232X
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