Variants in autophagy genes MTMR12 and FAM134A are putative modifiers of the hepatic phenotype in α1-antitrypsin deficiency.

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Title: Variants in autophagy genes MTMR12 and FAM134A are putative modifiers of the hepatic phenotype in α1-antitrypsin deficiency.
Authors: Tafaleng EN; Departments of Pediatrics, Surgery and Pathology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA., Li J; Departments of Pediatrics, Cell Biology and Physiology, Genetics and McDonnell Genome Institute, Washington University School of Medicine, St. Louis, Missouri, USA., Wang Y; Departments of Pediatrics, Surgery and Pathology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA., Hidvegi T; Departments of Pediatrics, Cell Biology and Physiology, Genetics and McDonnell Genome Institute, Washington University School of Medicine, St. Louis, Missouri, USA., Soto-Gutierrez A; Departments of Pediatrics, Surgery and Pathology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA., Locke AE; Departments of Pediatrics, Cell Biology and Physiology, Genetics and McDonnell Genome Institute, Washington University School of Medicine, St. Louis, Missouri, USA., Nicholas TJ; Departments of Pediatrics, Cell Biology and Physiology, Genetics and McDonnell Genome Institute, Washington University School of Medicine, St. Louis, Missouri, USA., Wang YC; Departments of Pediatrics, Cell Biology and Physiology, Genetics and McDonnell Genome Institute, Washington University School of Medicine, St. Louis, Missouri, USA., Pak S; Departments of Pediatrics, Cell Biology and Physiology, Genetics and McDonnell Genome Institute, Washington University School of Medicine, St. Louis, Missouri, USA., Cho MH; Channing Laboratories, Harvard Medical School, Boston, Massachusetts, USA., Silverman EK; Channing Laboratories, Harvard Medical School, Boston, Massachusetts, USA., Silverman GA; Departments of Pediatrics, Cell Biology and Physiology, Genetics and McDonnell Genome Institute, Washington University School of Medicine, St. Louis, Missouri, USA., Jin SC; Departments of Pediatrics, Cell Biology and Physiology, Genetics and McDonnell Genome Institute, Washington University School of Medicine, St. Louis, Missouri, USA., Fox IJ; Departments of Pediatrics, Surgery and Pathology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania, USA., Perlmutter DH; Departments of Pediatrics, Cell Biology and Physiology, Genetics and McDonnell Genome Institute, Washington University School of Medicine, St. Louis, Missouri, USA.
Source: Hepatology (Baltimore, Md.) [Hepatology] 2024 Oct 01; Vol. 80 (4), pp. 859-871. Date of Electronic Publication: 2024 Apr 01.
Publication Type: Journal Article; Research Support, N.I.H., Extramural
Journal Info: Publisher: Wolters Kluwer Health, Inc Country of Publication: United States NLM ID: 8302946 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1527-3350 (Electronic) Linking ISSN: 02709139 NLM ISO Abbreviation: Hepatology Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1527-3350
DOI:10.1097/HEP.0000000000000865