Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleA homozygous missense mutation in PEPD encoding peptidase D causes prolidase deficiency associated with hyper-IgE syndrome.AuthorsHershkovitz T; Hassoun G; Indelman M; Shlush LI; Bergman R; Pollack S; Sprecher EPublicationClinical and experimental dermatology, 2006, Vol 31, Issue 3, p435ISSN0307-6938Publication typearticleDOI10.1111/j.1365-2230.2006.02112.x