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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
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PubType: Academic Journal
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  Data: Clinical and biochemical characterization of a patient with prolidase deficiency, a rare disorder of collagen metabolism.
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  Data: <searchLink fieldCode="AU" term="%22Coody+TK%22">Coody TK</searchLink>; Department of Pathology, University of Utah, Salt Lake City, UT 84108, USA.<br /><searchLink fieldCode="AU" term="%22De+Biase+I%22">De Biase I</searchLink>; Department of Pathology, University of Utah, Salt Lake City, UT 84108, USA.<br /><searchLink fieldCode="AU" term="%22Porter+JM%22">Porter JM</searchLink>; Department of Pediatrics, Division of Medical Genetics, University of Utah, Salt Lake City, UT 84108, USA.<br /><searchLink fieldCode="AU" term="%22Pasquali+M%22">Pasquali M</searchLink>; 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.<br /><searchLink fieldCode="AU" term="%22Shayota+BJ%22">Shayota BJ</searchLink>; Department of Pediatrics, Division of Medical Genetics, University of Utah, Salt Lake City, UT 84108, USA.
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  Data: <searchLink fieldCode="JN" term="%22101624422%22">Molecular genetics and metabolism reports</searchLink> [Mol Genet Metab Rep] 2025 Sep 23; Vol. 45, pp. 101258. <i>Date of Electronic Publication: </i>2025 Sep 23 (<i>Print Publication: </i>2025).
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Elsevier+Inc%22">Elsevier Inc </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>101624422 <i>Publication Model: </i>eCollection <i>Cited Medium: </i>Print <i>ISSN: </i>2214-4269 (Print) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2222144269%22">22144269 </searchLink><i>NLM ISO Abbreviation: </i>Mol Genet Metab Rep <i>Subsets: </i>PubMed not MEDLINE
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        Value: 10.1016/j.ymgmr.2025.101258
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      – Code: eng
        Text: English
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        StartPage: 101258
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      – TitleFull: Clinical and biochemical characterization of a patient with prolidase deficiency, a rare disorder of collagen metabolism.
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            – D: 23
              M: 09
              Text: 2025 Sep 23
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