Dominant NARS1 mutations causing axonal Charcot-Marie-Tooth disease expand NARS1-associated diseases.

Saved in:
Bibliographic Details
Title: Dominant NARS1 mutations causing axonal Charcot-Marie-Tooth disease expand NARS1-associated diseases.
Authors: Beijer D; Translational Neurosciences, Faculty of Medicine and Health Sciences, University of Antwerp, Wilrijk, B-2610, Belgium.; Laboratory of Neuromuscular Pathology, Institute Born-Bunge, University of Antwerp, Wilrijk, B-2610, Belgium.; Department for Human Genetics and John P. Hussman Institute for Human Genomics, University of Miami, Miami, FL 33136, USA., Marte S; Department of Human Genetics, University of Michigan Medical School, Ann Arbor, MI 48109, USA., Li JC; The Jackson Laboratory, Bar Harbor, ME 04609, USA.; Genetics Program, Graduate School of Biomedical Sciences, Tufts University, Boston, MA 02111, USA., De Ridder W; Translational Neurosciences, Faculty of Medicine and Health Sciences, University of Antwerp, Wilrijk, B-2610, Belgium.; Laboratory of Neuromuscular Pathology, Institute Born-Bunge, University of Antwerp, Wilrijk, B-2610, Belgium.; Neuromuscular Reference Centre, Department of Neurology, Antwerp University Hospital, Wilrijk, B-2610, Belgium., Chen JZ; Department of Neurology, Austin Health, Melbourne, VIC 3084, Australia., Tadenev ALD; The Jackson Laboratory, Bar Harbor, ME 04609, USA., Miers KE; The Jackson Laboratory, Bar Harbor, ME 04609, USA., Deconinck T; Translational Neurosciences, Faculty of Medicine and Health Sciences, University of Antwerp, Wilrijk, B-2610, Belgium.; Center of Medical Genetics, University of Antwerp and Antwerp University Hospital, Edegem, B-2650, Belgium., Macdonell R; Department of Neurology, Austin Health, Melbourne, VIC 3084, Australia., Marques W Jr; Department of Neurosciences and Behavior Sciences, School of Medicine of Ribeirão Preto, University of São Paulo, São Paulo, SP, 14051-140, Brazil., De Jonghe P; Translational Neurosciences, Faculty of Medicine and Health Sciences, University of Antwerp, Wilrijk, B-2610, Belgium.; Laboratory of Neuromuscular Pathology, Institute Born-Bunge, University of Antwerp, Wilrijk, B-2610, Belgium.; Neuromuscular Reference Centre, Department of Neurology, Antwerp University Hospital, Wilrijk, B-2610, Belgium., Pratt SL; The Jackson Laboratory, Bar Harbor, ME 04609, USA.; Neuroscience Program, Graduate School of Biomedical Sciences, Tufts University, Boston, MA 02111, USA., Meyer-Schuman R; The Jackson Laboratory, Bar Harbor, ME 04609, USA., Züchner S; Department for Human Genetics and John P. Hussman Institute for Human Genomics, University of Miami, Miami, FL 33136, USA., Antonellis A; Department of Human Genetics, University of Michigan Medical School, Ann Arbor, MI 48109, USA.; Department of Neurology, University of Michigan Medical School, Ann Arbor, MI 48109, USA., Burgess RW; The Jackson Laboratory, Bar Harbor, ME 04609, USA.; Genetics Program, Graduate School of Biomedical Sciences, Tufts University, Boston, MA 02111, USA.; Neuroscience Program, Graduate School of Biomedical Sciences, Tufts University, Boston, MA 02111, USA., Baets J; Translational Neurosciences, Faculty of Medicine and Health Sciences, University of Antwerp, Wilrijk, B-2610, Belgium.; Laboratory of Neuromuscular Pathology, Institute Born-Bunge, University of Antwerp, Wilrijk, B-2610, Belgium.; Neuromuscular Reference Centre, Department of Neurology, Antwerp University Hospital, Wilrijk, B-2610, Belgium.
Source: Brain communications [Brain Commun] 2024 Mar 08; Vol. 6 (2), pp. fcae070. Date of Electronic Publication: 2024 Mar 08 (Print Publication: 2024).
Publication Type: Journal Article
Journal Info: Publisher: Oxford University Press Country of Publication: England NLM ID: 101755125 Publication Model: eCollection Cited Medium: Internet ISSN: 2632-1297 (Electronic) Linking ISSN: 26321297 NLM ISO Abbreviation: Brain Commun Subsets: PubMed not MEDLINE
Database: MEDLINE Ultimate
Full text is not displayed to guests.
Description
ISSN:2632-1297
DOI:10.1093/braincomms/fcae070