Clinical and biochemical characterization of a patient with prolidase deficiency, a rare disorder of collagen metabolism.

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Title: Clinical and biochemical characterization of a patient with prolidase deficiency, a rare disorder of collagen metabolism.
Authors: Coody TK; Department of Pathology, University of Utah, Salt Lake City, UT 84108, USA., De Biase I; Department of Pathology, University of Utah, Salt Lake City, UT 84108, USA., Porter JM; Department of Pediatrics, Division of Medical Genetics, University of Utah, Salt Lake City, UT 84108, USA., Pasquali M; Department of Pathology, University of Utah, Salt Lake City, UT 84108, USA.; Department of Pediatrics, Division of Medical Genetics, University of Utah, Salt Lake City, UT 84108, USA., Shayota BJ; Department of Pediatrics, Division of Medical Genetics, University of Utah, Salt Lake City, UT 84108, USA.
Source: Molecular genetics and metabolism reports [Mol Genet Metab Rep] 2025 Sep 23; Vol. 45, pp. 101258. Date of Electronic Publication: 2025 Sep 23 (Print Publication: 2025).
Publication Type: Case Reports; Journal Article
Journal Info: Publisher: Elsevier Inc Country of Publication: United States NLM ID: 101624422 Publication Model: eCollection Cited Medium: Print ISSN: 2214-4269 (Print) Linking ISSN: 22144269 NLM ISO Abbreviation: Mol Genet Metab Rep Subsets: PubMed not MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:2214-4269
DOI:10.1016/j.ymgmr.2025.101258