HINT1 neuropathy in Lithuania: clinical, genetic, and functional profiling.
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| Title: | HINT1 neuropathy in Lithuania: clinical, genetic, and functional profiling. |
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| Authors: | Malcorps M; Molecular Neurogenomics Group, VIB Center for Molecular Neurology, VIB, Antwerp, Belgium.; Molecular Neurogenomics Group, Department of Biomedical Sciences, University of Antwerp, Antwerp, Belgium., Amor-Barris S; Molecular Neurogenomics Group, VIB Center for Molecular Neurology, VIB, Antwerp, Belgium.; Molecular Neurogenomics Group, Department of Biomedical Sciences, University of Antwerp, Antwerp, Belgium., Burnyte B; Department of Human and Medical Genetics, Institute of Biomedical Sciences, Faculty of Medicine, Vilnius University, Vilnius, Lithuania., Vilimiene R; Institute of Clinical Medicine, Faculty of Medicine, Vilnius University, Vilnius, Lithuania., Armirola-Ricaurte C; Molecular Neurogenomics Group, VIB Center for Molecular Neurology, VIB, Antwerp, Belgium.; Molecular Neurogenomics Group, Department of Biomedical Sciences, University of Antwerp, Antwerp, Belgium., Grigalioniene K; Department of Human and Medical Genetics, Institute of Biomedical Sciences, Faculty of Medicine, Vilnius University, Vilnius, Lithuania., Ekshteyn A; Molecular Neurogenomics Group, VIB Center for Molecular Neurology, VIB, Antwerp, Belgium.; Molecular Neurogenomics Group, Department of Biomedical Sciences, University of Antwerp, Antwerp, Belgium., Morkuniene A; Department of Human and Medical Genetics, Institute of Biomedical Sciences, Faculty of Medicine, Vilnius University, Vilnius, Lithuania., Vaitkevicius A; Institute of Clinical Medicine, Faculty of Medicine, Vilnius University, Vilnius, Lithuania., De Vriendt E; Molecular Neurogenomics Group, VIB Center for Molecular Neurology, VIB, Antwerp, Belgium.; Molecular Neurogenomics Group, Department of Biomedical Sciences, University of Antwerp, Antwerp, Belgium., Baets J; Translational Neurosciences, Faculty of Medicine and Health Sciences, University of Antwerp, Antwerp, Belgium.; Laboratory of Neuromuscular Pathology, Institute Born-Bunge, University of Antwerp, Antwerp, Belgium.; Neuromuscular Reference Center, Department of Neurology, Antwerp University Hospital, Antwerp, Belgium., Scherer SS; Department of Neurology, The Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA., Ambrozaityte L; Department of Human and Medical Genetics, Institute of Biomedical Sciences, Faculty of Medicine, Vilnius University, Vilnius, Lithuania., Utkus A; Department of Human and Medical Genetics, Institute of Biomedical Sciences, Faculty of Medicine, Vilnius University, Vilnius, Lithuania., Jordanova A; Molecular Neurogenomics Group, VIB Center for Molecular Neurology, VIB, Antwerp, Belgium. Albena.jordanova@uantwerpen.vib.be.; Molecular Neurogenomics Group, Department of Biomedical Sciences, University of Antwerp, Antwerp, Belgium. Albena.jordanova@uantwerpen.vib.be.; Department of Medical Chemistry and Biochemistry, Medical University - Sofia, Sofia, Bulgaria. Albena.jordanova@uantwerpen.vib.be., Peeters K; Molecular Neurogenomics Group, VIB Center for Molecular Neurology, VIB, Antwerp, Belgium.; Molecular Neurogenomics Group, Department of Biomedical Sciences, University of Antwerp, Antwerp, Belgium. |
| Source: | Orphanet journal of rare diseases [Orphanet J Rare Dis] 2022 Oct 14; Vol. 17 (1), pp. 374. Date of Electronic Publication: 2022 Oct 14. |
| Publication Type: | Journal Article; Research Support, Non-U.S. Gov't; Research Support, N.I.H., Extramural |
| Journal Info: | Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium: Internet ISSN: 1750-1172 (Electronic) Linking ISSN: 17501172 NLM ISO Abbreviation: Orphanet J Rare Dis Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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