Prolidase deficiency: A novel PEPD missense variant in exon 2.
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| Title: | Prolidase deficiency: A novel PEPD missense variant in exon 2. |
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| Authors: | Ido F; Department of Pulmonary and Critical Care, St. Luke's University Health Network, Bethlehem, Pennsylvania, USA., Tessier S; Lewis Katz School of Medicine, Temple University, Philadelphia, Pennsylvania, USA., Yoder N; Department of Pulmonary and Critical Care, St. Luke's University Health Network, Bethlehem, Pennsylvania, USA., Ramzy J; Department of Pulmonary and Critical Care, St. Luke's University Health Network, Bethlehem, Pennsylvania, USA., Longo S; Department of Pathology, St. Luke's University Health Network, Bethlehem, Pennsylvania, USA. |
| Source: | American journal of medical genetics. Part A [Am J Med Genet A] 2023 May; Vol. 191 (5), pp. 1388-1394. Date of Electronic Publication: 2023 Feb 09. |
| Publication Type: | Case Reports; Journal Article |
| Journal Info: | Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1552-4833 (Electronic) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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