Autosomal recessive ELOVL1-related disorder presenting with severe neonatal cholestasis: A novel clinical feature?

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Bibliographic Details
Title: Autosomal recessive ELOVL1-related disorder presenting with severe neonatal cholestasis: A novel clinical feature?
Authors: Tsai AC; Division of Genetics, Department of Clinical Pediatrics, University of Illinois Chicago, 840 S. Wood Street, Chicago, IL 60612, USA., Lee HT; Division of Genetics, Department of Clinical Pediatrics, University of Illinois Chicago, 840 S. Wood Street, Chicago, IL 60612, USA.; College of Medicine, Taipei Medical University, No. 250 Wuxing Street, Taipei City 11031, Taiwan., Sanchez B; Department of Clinical Pediatrics, University of Colorado, 80045, USA., Huang YR; Department of Genetics and Genomic Sciences, Case Western Reserve University and University Hospitals, Cleveland, OH 44106, USA., Krysinski S; Division of Genetics, Department of Clinical Pediatrics, University of Illinois Chicago, 840 S. Wood Street, Chicago, IL 60612, USA., Zalan A; Division of Genetics, Department of Clinical Pediatrics, University of Illinois Chicago, 840 S. Wood Street, Chicago, IL 60612, USA., Falsey E; Division of Genetics, Department of Clinical Pediatrics, University of Illinois Chicago, 840 S. Wood Street, Chicago, IL 60612, USA.
Source: Molecular genetics and metabolism reports [Mol Genet Metab Rep] 2026 Mar 11; Vol. 47, pp. 101305. Date of Electronic Publication: 2026 Mar 11 (Print Publication: 2026).
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.2026.101305